Development and Transfer Agreement for Genetic Analysis Systems

Details

Parties

1

Definitions and interpretation

1.1

Definition

(a)

the accounting standards made by the Australian Accounting Standards Board in accordance with the Corporations Act, and the requirements of that Act relating to the preparation and content of accounts; and

(b)

generally accepted accounting principles that are consistently applied in Australia, except those inconsistent with the standards or requirements referred to in paragraph (a) of this definition.

(a)

machine learning algorithms for genetic variant interpretation;

(b)

personalized supplement and vitamin recommendations;

(c)

lifestyle modification suggestions based on genetic predispositions;

(d)

specialist referral recommendations based on genetic risk factors;

(e)

integration with current medical knowledge bases;

(f)

automatic updates to interpretation algorithms based on new research; and

(g)

user-friendly presentation of complex genetic information.

(a)

a rules-based pipeline that:

(i)

systematically applies established clinical guidelines;

(ii)

ensures compliance with industry standards;

(iii)

validates against known best-practice criteria;

(iv)

performs structured variant classification checks;

(v)

maintains auditable decision trails;

(b)

an LLM-based analysis system that:

(i)

utilizes LLM pre-trained models;

(ii)

automatically aggregates and curates genetic variant information from multiple sources including:

(a)

academic literature from PubMed;

(b)

NCBI databases;

(c)

OMIM entries;

(d)

GeneCards (or similar);

(e)

LitVar;

(f)

other relevant scientific databases;

(iii)

generates explanatory summaries and interpretations;

(iv)

provides context for variant classifications;

(c)

an integration layer that:

(i)

combines outputs from both systems;

(ii)

maintains HIPAA compliance in all data handling and storage;

(iii)

operates independently of external cloud services;

(iv)

provides comprehensive audit trails;

(v)

includes documentation for deployment and maintenance.

(a)

The Development Work;

(b)

The benefit of the Assistance Activities;

(c)

Technical documentation created specifically for these developments;

(d)

The Records related to these developments. For clarity, Assets specifically excludes:

(e)

Any pre-existing GenVue or Genetic Genie code, platforms, or systems

(f)

The GenVue and Genetic Genie brands and associated intellectual property

(g)

Any intellectual property not specifically created for this development project

(h)

Any systems, code, or materials developed by the Seller outside this specific project

(a)

technical training sessions, documentation reviews, code walkthroughs and detailed architecture explanations covering all aspects of Platform operation and development;

(b)

providing complete access to all development documentation, including architectural decisions, technical considerations and planned enhancement roadmaps including detailed explanations of system design choices, open source or other technology or software reliance, performance optimization strategies and known limitations or areas for improvement;

(c)

providing comprehensive documentation of all third-party dependencies, including licensing requirements, version compatibilities, and integration considerations;

(d)

assisting in the establishment of development workflows and procedures within the Buyer's organisation including guidance on development of best practices, code review procedures, testing methodologies and deployment strategies specific to the Platform and it’s future developments and iterations;

(e)

providing detailed documentation and training on all aspects of Platform maintenance, including routine maintenance procedures, monitoring requirements and troubleshooting guidelines including comprehensive documentation of all system dependencies, scheduled maintenance requirements and performance optimisation procedures;

(f)

assisting in establishing monitoring and alerting systems to ensure continued existing and future iterations, platform stability and performance;

(g)

providing support for critical issue resolution, including assistance with bug fixes, security patches and performance optimisation including guidance on implementing system updates, managing database migrations and maintaining system security;

(h)

providing documentation of known issues, workarounds, and planned resolutions for any existing technical deficiencies;

(i)

providing consultation, conceptualisation and guidance on planned Platform enhancements and future development initiatives including sharing insights on potential feature enhancements, scalability considerations and technology evolution strategies as well as documentation of planned development initiatives, including technical specifications and implementation considerations for features contemplated or currently in development;

(j)

guidance on integrating new technologies, implementing system improvements and maintaining compatibility with evolving industry standards;

(k)

providing specific guidance on:

(i)

best practices for implementing new analysis modules;

(ii)

methods for extending the Platform's data models;

(iii)

approaches for integrating new screening capabilities;

(iv)

strategies for maintaining system performance with additional functionalities;

(v)

recommendations for scaling the Platform to accommodate new features; and

(l)

answering questions, providing guidance, resolving issues and assisting with transition and future development activities.

(a)

implementation of permanent backlinks from relevant pages;

(b)

development of contextual linking systems;

(c)

strategic placement of links within the navigation structure;

(d)

maintenance of link integrity and relevance.

(a)

the terms of this document and its subject matter, including information submitted or disclosed by a party during negotiations, discussions and meetings relating to this document;

(b)

information that at the time of disclosure by a disclosing party is identified to the receiving party as being confidential; and

(c)

all other information belonging or relating to a disclosing party that is not generally available to the public at the time of disclosure other than by reason of a breach of this document or which the receiving party knows, or ought reasonably to be expected to know, is confidential to that disclosing party or any Related Entity of that disclosing party.

(a)

▇▇▇▇’s Consideration Shares;

(a)

All software, systems, and deliverables created specifically under this agreement, including:

(i)

the Backlink Services implementation;

(ii)

the LIMS System;

(iii)

the Supplement Recommendation System;

(iv)

the Pregnancy Support Module;

(b)

All associated materials created specifically for these developments:

(i)

source code and documentation;

(ii)

algorithms and analytical methods;

(iii)

user interfaces and implementations;

(iv)

database schemas and data models;

(v)

customized workflows and business logic;

(vi)

integration protocols and configurations;

(vii)

testing and validation procedures;

(viii)

deployment and maintenance documentation;

(c)

The Records related to these developments.

(d)

Any pre-existing GenVue or Genetic Genie code, platforms, or systems

(e)

The GenVue and Genetic Genie brands and associated intellectual property

(f)

Any intellectual property not specifically created for this development project

(g)

Any systems, code, or materials developed by the Seller outside this specific project

(a)

any security for the payment of money or performance of obligations;

(b)

any legal or equitable interest or power reserved in or over an interest in an asset, including any retention of title;

(c)

any PPSA Security Interest;

(d)

an interest or power created or arising in or over an interest in an asset under a bill of sale, mortgage, charge, lien, pledge, hypothecation, preferential right, trust or other similar instrument, device or power; or

(e)

any other adverse right, title or interest of any nature, by way of security for the payment of a debt or the performance of any other obligation,

(a)

any patents, utility models, copyrights, registered or unregistered trade marks or service marks, trade names, brand names, indications of source or appellations of origin, eligible layout rights, plant variety rights, registered designs and commercial names and designations;

(b)

any invention, discovery, trade secret, know-how, computer software and confidential, scientific, technical and product information;

(c)

any other rights resulting from intellectual activity in the industrial, scientific, literary and artistic fields whether industrial, commercial, agricultural or extractive and whether dealing with manufactured or natural products; and

(d)

any letters patent, deed of grant, certificate or document of title for any thing referred to in paragraphs (a), (b) or (c) of this definition and any medium in which any thing referred to in those paragraphs is stored or embodied.

(a)

API-based integration with external laboratory centers;

(b)

sample tracking and management capabilities;

(c)

standardized data format conversion and validation;

(d)

chain of custody tracking and documentation;

(e)

quality control metrics and reporting;

(f)

results delivery automation.

(a)

All systems developed under this agreement;

(b)

Associated user interfaces and backend infrastructure;

(c)

Security implementations and data protection systems;

(d)

API integrations and frameworks;

(e)

Documentation and technical materials;

(f)

Development environments and deployment configurations.

(g)

The existing GenVue and Genetic Genie platforms

(h)

Pre-existing code and systems

(i)

Seller's independent developments outside this project

(j)

The GenVue and Genetic Genie brands

(a)

all documentation in respect of:

(i)

the Platform's extensibility framework;

(ii)

API integration points for new functionality;

(iii)

data model expansion capabilities;

(iv)

workflow customization mechanisms;

(v)

integration patterns for new analysis modules;

(b)

complete technical specifications, architecture diagrams, API documentation, data schemas, deployment configurations and operational procedures accompanied by all source code repositories, including full version control history, build scripts, deployment procedures and testing frameworks;

(c)

all configuration files, scripts and documentation necessary for building, testing, deploying and maintaining the Platform.

(a)

software, source code, object code, algorithms, development tools, files, records, documentation, and data comprising or relating to the Platform;

(b)

inventions, innovations, improvements, developments, methods, designs, analyses, drawings, reports, and all similar or related information (whether or not patentable) comprising or relating to the Platform;

(c)

patents, patent applications, and patent disclosures, together with all reissuances, continuations, continuations-in-part, revisions, extensions, and re-examinations thereof;

(d)

trademarks, service marks, trade dress, logos, trade names, corporate names, and domain names, and all goodwill associated therewith;

(e)

copyrights, mask works, and copyrightable works, and all applications, registrations, and renewals in connection therewith;

(f)

trade secrets and confidential business information (including ideas, research and development, know-how, formulas, compositions, manufacturing and production processes and techniques, technical data, designs, drawings, specifications, user and supplier lists, pricing and cost information, and business and marketing plans and proposals);

(g)

computer software (including data, databases, and related documentation);

(h)

other proprietary rights;

(i)

copies and tangible embodiments thereof (in whatever form or medium); and

(j)

rights to extend, modify, enhance or add new functionalities to the Platform, including but not limited to:

(i)

carrier screening capabilities;

(ii)

cancer screening result integration;

(iii)

microbiome analysis;

(iv)

additional genomic analysis tools;

(v)

integration with external diagnostic data sources;

(vi)

expansion of analytical capabilities to new areas of genetic testing;

(vii)

development of new screening methodologies; and

(viii)

any other genomic or medical analysis capabilities

(ix)

incentivised sharing

(x)

data collection and AI/LLM integrations.

(a)

pregnancy-specific supplement and vitamin recommendations based on genetic analysis;

(b)

IVF support supplementation protocols tailored to genetic profiles;

(c)

timing recommendations for supplementation during pregnancy and IVF cycles;

(d)

integration with existing pregnancy and IVF treatment protocols;

(e)

identification of genetic factors relevant to fertility and pregnancy;

(f)

automated product recommendations with affiliate linking capability.

(a)

custom user interface designs and implementations;

(b)

specific database schemas and data models;

(c)

customized workflows and business logic;

(d)

portal-specific integrations and configurations;

(e)

documentation specific to the portal implementation; and

(f)

any other development work performed specifically for the portal instance.

(a)

literature, brochures and other promotional material;

(b)

de-identified lists of all users and their genetic library inputs;

(c)

lists of all suppliers; and

(d)

records of and relating to the Contracts.

(a)

all rights subsisting (including associated reputation and goodwill) in:

(i)

the Platform Intellectual Property Rights;

(ii)

the domain names, trade marks and other intellectual property described in Schedule 2;

(b)

all rights subsisting in the Seller in trade secrets and in financial, marketing and technical information, ideas, concepts, know-how, technology, processes and knowledge which is confidential or of a sensitive nature (but excluding that which is in the public domain) used by the Seller in the Platform or Development of the Platform or in connection with the Assets; and

(c)

all other Intellectual Property Rights (excluding moral rights) owned by the Seller and used in the connection with the Assets or Platform.

(a)

AI/LLM/algorithmic analysis of genetic variants for supplement needs;

(b)

integration with product databases;

(c)

automated recommendation generation;

(d)

user-friendly presentation of recommendations;

(e)

affiliate linking capabilities where applicable.

1.2

Interpretation

(a)

A reference to:

(i)

one gender includes every other gender;

(ii)

the singular includes the plural and the plural includes the singular;

(iii)

a person includes a body corporate or unincorporate;

(iv)

a party includes the party’s executors, administrators, successors and permitted assigns;

(v)

a statute, regulation or provision of a statute or regulation (Statutory Provision) includes:

(A)

that Statutory Provision as amended or re-enacted from time to time;

(B)

a statute, regulation or provision enacted in replacement of that Statutory Provision; and

(C)

another regulation or other statutory instrument made or issued under that Statutory Provision; and

(vi)

money is to Australian dollars, unless otherwise stated.

(b)

The expression “this document” includes the deed, covenants, agreement, arrangement, understanding or transaction recorded in this document.

(c)

“Including” and similar expressions are not words of limitation.

(d)

A reference to a clause or schedule is a reference to a clause of or a schedule to this document.

(e)

A reference to a document (including, without limitation, a reference to this document) is to that document as amended, novated or replaced.

(f)

Where a word or expression is given a particular meaning, other parts of speech and grammatical forms of that word or expression have a corresponding meaning.

(g)

Headings and any table of contents or index are for convenience only and do not form part of this document or affect its interpretation.

(h)

A provision of this document must not be construed to the disadvantage of a party merely because that party was responsible for the preparation of this document or the inclusion of the provision in this document.

(i)

An agreement, representation or warranty in favour of two or more persons is for the benefit of them jointly and severally.

(j)

If an act must be done on a specified day which is not a Business Day, it must be done instead on the next Business Day.

(k)

All references to time are to Australian Eastern Standard time.

1.3

Parties

(a)

If a party is made up of more than one person, or a term is used in this document to refer to more than one party, then:

(i)

a reference to a party includes each and every person;

(ii)

those persons are bound separately; and

(iii)

any two or more persons are bound jointly and severally.

(b)

A party which is a trustee of a trust is bound in its personal capacity and in its capacity as trustee.

1.4

Best and reasonable efforts

(a)

(payment) to pay any money, or to provide any financial compensation, valuable consideration or any other incentive to or for the benefit of any person; or

(b)

(legal action) to commence any legal action against any person, to procure that that thing is done or happens;

(c)

(fees) for payment of any applicable fee for the lodgement or filing of any relevant application with any Government Agency; or

(d)

(contrary provision) where that provision expressly specifies otherwise.

2

Agreement for development

2.1

Development Scope and Rights

(a)

The Seller agrees to develop and implement only the following new components:

(i)

LIMS System

(ii)

AI Interpretation System

(iii)

Supplement Recommendation System

(iv)

Pregnancy Support Module

(v)

AI Variant Curator

(b)

The Seller will:

(i)

deliver source code and documentation for these specific new components only;

(ii)

transfer ownership of only the newly created work specific to these components;

(iii)

provide implementation support for these specific components.

(c)

For absolute clarity:

(i)

Only newly created code and developments for these specified systems are included

(ii)

All pre-existing code, platforms, and IP remain the sole property of the Seller

(iii)

The GenVue and Genetic Genie platforms, brands, and IP are explicitly excluded

(iv)

Any improvements or modifications to pre-existing Seller IP remain owned by Seller

(d)

provide implementation and maintenance rights

(e)

For clarity, this agreement covers only:

(i)

Newly created code and developments for the specified systems

(ii)

Documentation specific to these new developments

(iii)

Technical materials created specifically for these systems

(ii)

Pre-existing intellectual property

(iii)

The GenVue and Genetic Genie brands

(iv)

Any systems or code not specifically created for this project

2.2

No Encumbrances

2.3

Title and Risk

(a)

The Seller:

(i)

Retains full ownership of all pre-existing IP

(ii)

Retains all rights to GenVue and Genetic Genie platforms

(iii)

Maintains unrestricted right to develop pre-existing IP

(iv)

Retains all associated brands and trademarks

(b)

The Buyer obtains ownership only of:

(i)

Newly created code for specified components

(ii)

Documentation created specifically for new components

(iii)

Customizations made specifically for this project

(c)

For clarity, the Buyer obtains no rights to:

(i)

Pre-existing Seller IP

(ii)

Seller's platforms or brands

(iii)

Improvements to Seller's pre-existing IP

2.4

Application for Consideration Shares

(a)

For the purposes of the Constitution, this document serves as an application by the Seller for the Consideration Shares on the date of execution of this document.

(b)

Each Seller agrees to be bound by the Constitution upon the issue of the Consideration Shares by the Company to the Seller.

3

Consideration

3.1

Consideration Shares

3.2

Issue of Consideration Shares

(a)

On Completion the Buyer must:

(i)

issue the Consideration Shares to ▇▇▇▇ ▇▇▇;

(ii)

issue a share certificate in favour of ▇▇▇▇ ▇▇▇ in respect of the Consideration Shares.

(b)

As soon as practicable after Completion, the Buyer must register ▇▇▇▇ ▇▇▇ as the holder of the Consideration Shares.

3.3

Apportionment

Asset

Value

Platform development

USD$ 1,799,995.00

The benefit of  the Assistance Activities

USD$1.00

Seller Intellectual Property Rights

USD$1.00

Contracts

USD$1.00

Records

USD$1.00

Goodwill

USD$1.00

3.4

Goodwill

4

Conduct of operation pending Completion

4.1

Platform performance

(a)

(operational activity) continue to carry on the Platform in the ordinary and usual course;

(b)

(protection) perform any action within its power and control to maintain profitability and value of the Assets and the Platform;

(c)

(Goodwill) maintain the current operational relationships and ▇▇▇▇▇▇▇▇;

(d)

(grant an interest) not grant any interest in any Seller Intellectual Property Rights;

(e)

(maintain Seller Intellectual Property Rights) not cancel or fail to renew any registration of

(f)

do anything which materially prejudices the likelihood of Completion occurring

4.2

Restricted Action

(a)

(disposal) dispose of, agree to dispose of, encumber or grant an option over any Asset; or

(b)

(extraordinary commitments) enter into or incur on behalf of the Platform, any commitments or liabilities, other than commitments or liabilities in the ordinary course of business.

5

Completion

5.1

Location and time

5.2

Seller’s obligations on Completion

(a)

On Completion, the Seller hereby, with effect from Completion:

(ii)

transfers and assigns all right, title and interest in the Portal Implementation Work to the Buyer;

(b)

At Completion, the Seller must do all of the following:

(i)

(documentation) deliver to the Buyer copies of all documentation relating to the Development Rights;

(ii)

(Assets) deliver to the Buyer those Assets capable of delivery at the respective places where they are located;

(ii)

(title documents) deliver to the Buyer all certificates of title, registration certificates and other documents relating to the ownership and use of the Assets;

(iii)

(Assets) deliver to the Buyer those Assets capable of delivery at the respective places where they are located;

(iii)

(Platform Documentation) deliver the Platform Documentation to the Buyer in a format that is readily accessible and understandable by competent technical personnel, with sufficient detail to enable independent operation and further development of the Platform, and otherwise in a format satisfactory to the Buyer.

(iv)

(Third Party Components) where the consent of a third party is required, the Seller must, at the Seller's expense, assign or novate to the Buyer with effect on Completion any Third Party Component required by the Buyer.

(v)

(certificates of registration) deliver to the Buyer current certificates of registration in respect of those items of the Assets which are required to be registered with any public authority together with such duly signed licenses as will enable the Buyer to be registered with all such public authorities as the holder of current registration of each such item;

(vi)

(Contracts) in respect of those Contracts requiring the consent of any third party, deliver to the Buyer duly executed deeds of assignment or novation (as required) of the Contracts to the Buyer together with an original counterpart of each Contract in a form and substance reasonably satisfactory to the Buyer;

(vii)

(assignment of Seller Intellectual Property Rights) deliver to the Buyer a duly executed assignment of each item of the Seller Intellectual Property Rights together with the written consent to the assignment of all necessary persons in a form and substance reasonably satisfactory to the Buyer;

(viii)

(discharge) deliver to the Buyer discharges in the usual form of all Encumbrances granted by the Seller over any Asset to secure the obligations of the Seller to a lender or financier; and

5.3

Buyer’s obligations at Completion

(a)

(Consideration Shares) issue the Consideration Shares in accordance with clause 3.1;

(b)

(documents) accept all the documents and other items specified in clause 5.2 (Seller’s obligations on Completion); and

(c)

do all other acts and execute all other documents that this document requires the Buyer to do or execute at Completion.

5.4

Completion action

(a)

(Timing) Any action, including satisfaction of any condition precedent, performed by any party for the purpose of Completion is conditional upon and must be treated as simultaneous with performance of any action required to be performed by any other party for that purpose.

(b)

(Mutuality) Any action required to be performed by any party for the purpose of Completion must not be treated as performed or completed until performance or completion of all action required to be performed by each other party for that purpose.

5.5

Waiver of moral rights and Seller assistance

(a)

To the extent permitted by applicable law, the Seller hereby irrevocably waives all moral rights arising under the Copyright Act 1968 (Cth) or any similar laws of any jurisdiction in respect of the Seller Intellectual Property Rights.

(b)

The Seller agrees to provide to the Buyer any assistance necessary in any proceedings or applications for protection of the Seller Intellectual Property Rights.

6

Seller assistance

6.1

Acknowledgement

(a)

each party comprising the Seller provides consultancy or employment services to the Buyer pursuant to the terms of a consultancy or employment agreement between that party and the Buyer (each a Relevant Agreement);

(b)

the obligations of each party comprising the Seller set out in this clause 6 shall be performed in accordance with the terms of the Relevant Agreement relating to that party, subject to clause 6.1(c); and

(c)

the Seller shall not be remunerated for carrying out the Assistance Activities in satisfaction of its obligations under this clause 6.

6.2

Agreement

(a)

to undertake and provide, at the Sellers’ cost, the Assistance Activities until the earlier of the date that is 2 years from the Completion Date or until the date on which the Buyer gives notice in writing to the Seller that the Assistance Activities have been completed in accordance with this document and to the satisfaction of the Buyer (Assistance Period);

(b)

to conduct the Assistance Activities at such times and in such a manner as reasonably required by the Buyer;

(c)

to complete the Assistance Activities to the satisfaction of the Buyer before the date that is 2 years from the Completion Date;

(d)

(d) In the event a Seller ceases to be a contractor or employee of the Buyer prior to the completion of the Assistance Period ("Departing Seller"):

6.3

Post Assistance Period

6.4

Survival

7

Apportionment of expenses and income

7.1

Entitlement to income

(a)

the Seller is entitled to:

7.2

Unpaid goods and services

7.3

Prepaid goods and services

7.4

Apportionment of outgoings

7.5

Book debts

(a)

will be received by the Buyer as agent of the Seller and must be paid to the Seller; and

(b)

must be applied to reduce the Seller’s book debts in priority to debts owing to the Buyer.

8

Future Development Restrictions

8.6

Brand Protection

(a)

Nothing in this agreement grants the Buyer any rights to:

(i)

The GenVue name or brand

(ii)

The Genetic Genie name or brand

(iii)

Any associated trademarks or intellectual property

(b)

The Buyer shall not:

(i)

Use the GenVue or Genetic Genie names

(ii)

Market itself as associated with GenVue or Genetic Genie

(iii)

Represent that its platform is GenVue or Genetic Genie

(c)

The Seller retains all rights to the GenVue and Genetic Genie brands and may continue to use, develop, and market these brands independently

9

Seller warranties and indemnities

9.1

Seller warranties

9.2

Separate warranty

9.3

Seller indemnity

(a)

The Seller indemnifies the Buyer against any Claim to the extent that the Claim arises from or is connected with a breach of any of the Seller’s warranties.

(b)

The Seller shall not indemnify the Buyer for any claims arising from the Buyer’s failure to implement the Development Work in compliance with regulatory, healthcare, or legal standards.

9.4

Additional Licensing Warranties

9.5

Limitation of Liability

(a)

The Buyer acknowledges that it bears all liability and responsibility for:

(i)

Implementation and deployment of the Platform

(ii)

Regulatory and healthcare compliance

(iii)

Medical advice and recommendations

(iv)

User data protection

(v)

System modifications and enhancements

(vi)

Integration with third-party systems

(b)

The Seller's liability under this agreement shall be limited to:

(i)

Delivery of the specified Development Work

(ii)

Providing documentation and assistance as specified

(iii)

Warranty of non-infringement of third-party IP rights

(c)

In no event shall the Seller be liable for:

(i)

The Buyer's use or implementation decisions

(ii)

Medical or healthcare outcomes

(iii)

Regulatory compliance issues

(iv)

Data protection or privacy issues

(v)

System modifications by the Buyer

10

Seller acknowledgments

(a)

this document does not constitute a recommendation or financial product advice and the Company has not had regard to Sellers particular objectives, financial situation and needs;

(b)

except for any liability which cannot be excluded by law, the Company, its officers and affiliates do not make any warranty or representation as to the accuracy or completeness of any information given to the Seller or which is publicly available. The Company, its officers and affiliates exclude and disclaim all liability (including but not limited to fault or negligence) for any expense, loss, damage or cost that may be incurred by the Seller or any other person as a result of that information being inaccurate or incomplete in any way for any reason to the maximum extent permitted by law;

(c)

the Company is contracting on an arm’s-length basis with the Seller and the Seller is solely responsible for making their own independent judgement in relation to Consideration Shares and any other matters arising in connection with it and the this document does not create any obligation (fiduciary or otherwise) on the Company, its officers and affiliates. No duty of care is owed by the Company, its officers and affiliates to the Seller;

(d)

the Seller are aware that the acquisition, ownership and disposition of the Consideration Shares may have tax consequences in Australia and other applicable jurisdictions, which could negatively impact any return realised from the acquisition, ownership or disposition of the Consideration Shares. Any discussions of tax issues in information provided by the Company or officers are not intended to be legal or tax advice to any person and are not intended to be used, and cannot be used, by any person for the purpose of avoiding any tax penalties that may be imposed on that person. The Seller acknowledges that it is the Seller’ responsibility to consult with the Seller’ tax adviser or other professional adviser on tax aspects of the Seller acquisition, ownership and disposal of the Consideration Shares.

(e)

if restrictions on sale apply to the Consideration Shares, matching restrictions on transfer may be imposed;

(f)

an investment in the Consideration Shares involves a degree of risk. The Seller has considered the risks associated with the Consideration Shares in deciding whether to accept the Consideration Shares as consideration;

(g)

any expenses incurred by the Seller in relation to the Consideration Shares will be to the Seller’ own account; and

(h)

no prospectus, product disclosure statement, offering memorandum or other form of disclosure document has been prepared for lodgement or will be lodged with ASIC or other securities regulatory body in connection with the issue of the Consideration Shares.

11

Disputes

11.1

Notice

11.2

Best efforts to resolve

11.3

Arbitration

(a)

If the parties are not able to reach a resolution of the dispute or complaint within a reasonable period of time (in any event being no more than 21 days after the date of receipt of the notice of the complaint or dispute), then the dispute or complaint must be submitted for arbitration in accordance with, and subject to, the Resolution Institute Arbitration Rules.

(b)

For disputes which involve a Claim for less than $50,000.00, arbitration will take place by way of written submissions supported by relevant documents alone unless both parties agree otherwise.

11.4

Continuing obligations

12

Notices

12.1

Form

12.2

Delivery

(a)

sent by email to the email address set out or referred to in the Details; or

(b)

left at the address set out or referred to in the Details; or

(c)

sent by prepaid post to the address set out or referred to in the Details.

12.3

When effective

12.4

Receipt – email

12.5

Receipt – postal

12.6

Receipt – general

13

Confidentiality

13.1

Non disclosure

13.2

Protection

13.3

Disclosures required by law

13.4

Survival

14

Entire agreement

15

General

15.1

Amendments

15.2

Assignment

15.3

Consents

15.4

Survival of indemnities

15.5

Counterparts

(a)

This document may be entered into in any number of counterparts.

(b)

A party may execute this document by signing any counterpart.

(c)

All counterparts, taken together, constitute one document.

(d)

Each party consents to the exchange of counterparts of this document by delivery of a PDF document by email, or such other electronic means as may be agreed in writing.

15.6

Electronic Signature

(a)

The parties consent to this document being signed by or on behalf of a party by an Electronic Signature, if the document can be validly executed by an Electronic Signature in the jurisdiction specified in clause 17 (Governing law and jurisdiction).

(b)

Where this document is electronically signed by or on behalf of a party, the party warrants and agrees that the Electronic Signature has been used to identify the person signing and to indicate that the party intends to be bound by the Electronic Signature.

(c)

Clause 15.5 (Counterparts) applies to the execution and exchange of counterparts of this document that have been electronically signed.

(d)

In this clause 15.6, ‘Electronic Signature’ means a digital signature or a visual representation of a person’s handwritten signature or mark which is placed on a physical or electronic copy of this document by electronic or mechanical means, and “electronically signed” has a corresponding meaning.

15.7

Costs

(a)

Each party will bear its own costs and disbursements of or incidental to the negotiation, preparation and execution of this document, and all other matters and agreements referred to in this document.

(b)

The Buyer will pay for any stamp duty payable with respect to this document, and all other matters and agreements referred to in this document.

15.8

Further acts and documents

15.9

Waivers

15.10

Severance

(a)

If anything in this document is unenforceable, illegal or void then it is severed and the rest of this document remains in force, unless the severance would change the underlying principal commercial purpose or effect of this document.

(b)

If two or more provisions of this document are inconsistent or contradictory the numerical position of those provisions must not be a determinative factor in any decision, order or ruling that results in the severance of any conflicting provision.

15.11

Force Majeure

16.1

Notice to Complete

(c)

Subject to clause 15.10(d), without derogating from or limiting its rights at law or under this document, if the Seller or the Buyer (Non-Defaulting Party) does not complete on the Completion Date as a result of default of this document by the other (Defaulting Party), then the Non-Defaulting Party may give the Defaulting Party a notice requiring the Defaulting Party to complete within 10 Business Days after receipt of the notice.

(d)

Nothing in clause 15.10(c) limits the Non-Defaulting Party's rights in relation to a default by the Defaulting Party.

(e)

The Non-Defaulting Party is entitled to make a Claim against the defaulting party for any Loss suffered or incurred as a result of or in connection with the failure of the Defaulting Party to complete on the Completion Date.

16.2

Mitigation

16.3

Interest

16.4

Liability Allocation

(a)

The Buyer assumes full responsibility and liability for:

(i)

Implementation and deployment decisions

(ii)

Regulatory and healthcare compliance

(iii)

Medical recommendations and outcomes

(iv)

Data protection and privacy

(v)

System modifications and enhancements

(vi)

Integration with third-party systems

(b)

The Seller's liability is strictly limited to:

(i)

Delivery of specified Development Work

(ii)

Documented assistance obligations

(iii)

Non-infringement of third-party IP rights

(c)

The Buyer shall indemnify and hold harmless the Seller from:

(i)

Implementation decisions

(ii)

Regulatory compliance issues

(iii)

Medical or healthcare outcomes

(iv)

Data protection or privacy issues

(v)

System modifications or enhancements

(vi)

Third-party claims arising from ▇▇▇▇▇'s use or deployment

(d)

The Seller specifically disclaims all liability for:

(i)

Medical or healthcare outcomes

(ii)

Supplement recommendations and interactions

(iii)

Healthcare regulatory compliance

(iv)

Clinical or medical use of the system

(v)

Data protection and privacy compliance

(vi)

Implementation decisions by the Buyer

(e)

The Buyer agrees to defend, indemnify and hold harmless the Seller from any claims arising from:

(i)

Medical or healthcare outcomes

(ii)

Regulatory compliance issues

(iii)

Clinical implementation decisions

(iv)

Data protection violations

(v)

Modification of system disclaimers or warnings

16.5

Termination for Material Breach

(i)

The Buyer must return all Confidential Information and materials delivered by the Seller;

(ii)

The Seller must complete the transfer of any partially completed Development Work; and

(iii)

Both parties must continue to comply with confidentiality and indemnity obligations.

17

Governing law and jurisdiction

17.1

Governing law

17.2

Jurisdiction

(a)

The Seller makes no representation or warranty regarding the regulatory compliance, medical efficacy, or safety of the Development Work. The Buyer is solely responsible for validating all medical or supplement recommendations, ensuring compliance with healthcare regulations, and maintaining appropriate disclaimers and warnings to end users.

1.

Limitation of Warranties

(a)

All warranties in this Schedule:

(i)

Apply only to newly created Development Work

(ii)

Are void if the Buyer modifies the delivered code

(iii)

Are contingent on the Buyer's proper implementation

(iv)

Exclude any pre-existing Seller IP or platforms

(v)

Are subject to proper maintenance of all disclaimers and warnings

(b)

The Seller specifically disclaims any warranties regarding:

(i)

Medical or healthcare outcomes

(ii)

Regulatory compliance

(iii)

Clinical implementation

(iv)

Data protection

(v)

System modifications by the Buyer

2.

The Buyer

(a)

All warranties provided in this Schedule are subject to the system being used in accordance with provided documentation and guidelines;

(b)

The Buyer assumes all liability and responsibility for:

(i)

Implementation and deployment decisions

(ii)

Regulatory compliance in deployment

(iii)

Medical and healthcare compliance

(iv)

Maintaining appropriate disclaimers and warnings

(v)

User data protection and privacy

(vi)

System modifications made by the Buyer

(c)

The Seller's warranties extend only to the delivery of the specified Development Work in accordance with documented specifications, and do not cover:

(i)

Modifications made by the Buyer

(ii)

Integration with third-party systems by the Buyer

(iii)

Usage outside documented parameters

(iv)

Failure to maintain required disclaimers or warnings

3.

The Seller

(a)

The Seller is authorised to conduct development throughout the jurisdictions in which the Platform is conducted.

(b)

The Seller has full power and authority to own the Assets and conduct the Platform.

(c)

The Seller is not insolvent or bankrupt, and no controller or trustee has been appointed over any part of the Assets, and no appointment has been threatened.

(d)

The Seller is not in liquidation or administration, no proceedings have been brought or threatened and no procedure has been commenced for the purpose of winding up the Seller or placing it under administration.

(e)

Each party comprising the Seller enters into this document in its own capacity and not as trustee for any trust.

4.

Due authorisations

(a)

The execution and delivery of this document has been properly authorised by all necessary action of the Seller.

(b)

The Seller has full power and lawful authority to execute and deliver this document and to perform its obligations under this document.

(c)

This document and Completion do not conflict with, or result in a breach of, or default under, any provision or any material term or provision of any agreement, deed, law or order by which the Seller is bound.

5.

Shares

(a)

The Seller is in compliance with all relevant laws and regulations applicable to subscription of the Consideration Shares (including, without limitation, the requirements of the Corporations Act, the Foreign Acquisitions and Takeovers Act 1975 (Cth), the Competition and Consumer Act 2010 (Cth) and the constitution of the Company and the Seller will not cease to be in compliance if the Seller acquires the Consideration Shares.

(b)

The Seller has made and relied upon their own assessment of the Company and have conducted their own investigations with respect to the Consideration Shares including, without limitation, any restrictions on resale of the Consideration Shares and the particular tax consequences of acquiring, owning or disposing of the Consideration Shares in light of the Sellers particular situation and the Seller has decided to acquire the Consideration Shares based on the Sellers’ own enquiries and professional advice, and not in reliance upon any act, investigation, research, recommendation or representation made by the Company, its officers or any persons acting on behalf of them. None of those persons has made any representation to the Seller, express or implied, with respect to the Consideration Shares.

(c)

The Seller has knowledge and experience in financial matters such that the Seller are capable of evaluating the merits and risks of acquiring the Consideration Shares. The Seller has determined that the Consideration Shares are a suitable investment for the Seller both in the nature and number of the Consideration Shares being acquired. The Seller can bear the economic risk of an investment in the Consideration Shares.

(d)

The Seller has access to all information that the Seller believes is necessary or appropriate in connection with the Sellers’ acquisition of the Consideration Shares for an adequate time so as to enable the Seller to make an informed investment decision regarding the acquisition of the Consideration Shares.

6.

Accuracy of information

(a)

All information that has been given by, or on behalf of, the Seller to the Buyer in relation to the Platform and Assets is true, complete and accurate in all respects;

(b)

All information that the Seller knows about the Platform or the Assets which needs to be known by a buyer of the Platform, has been disclosed to the Buyer in writing;

(c)

All information given by the Seller or its professional advisers by or on behalf of the Seller to the Buyer or its professional advisers in the course of negotiations leading to this Agreement and Completion and the facts set out in the schedules to this Agreement are true, accurate and not misleading in all respects.

(d)

The Seller has disclosed to the Buyer all of the information that is reasonably within the possession of the Seller at the date of this document about the Platform and the Assets that a prudent purchaser for value would desire to know in the ordinary course of Platform and the information disclosed is true, complete and accurate and is not misleading (including by omission).

(e)

No circumstance has arisen, nor has any information become available prior to the date of this document, which has materially and adversely affected, or may materially and adversely affect, the Platform or the Assets.

(f)

All Records have been properly maintained in all material respects, are in the possession or control of the Seller, and give a materially accurate view of the matters which appear in them.

7.

Title

(a)

The Seller is the sole legal and beneficial owner of the Platform and of all the Assets.

(b)

The Seller has full rights, title and interest in the Platform and all the Assets, free from any Encumbrance or third-party interest.

(c)

The Seller has not disposed of, or agreed to dispose of, any of the Assets or any interest in any of the Assets other than to the Buyer.

8.

Financial Position

(a)

All information concerning the financial position of the Platform which has been shown by or on behalf of the Seller to the Buyer has been compiled in accordance with all applicable laws and regulations (including accounting standards, practices and policies).

(b)

There are no actual or contingent liabilities of, or unascertained Claims against, the Seller (including contractual commitments) which could materially and adversely affect the value of the Platform, the Assets or the Buyer's ability to conduct the Platform.

(c)

To the best of the Seller’s knowledge, information and belief all accounts, books, ledgers and financial or other records of the Seller which relate to the Platform:

(i)

have been fully and properly maintained and contain due records of all matters required to be entered by any relevant legislation or prudent Platform practice;

(ii)

do not contain or reflect any material inaccuracies or discrepancies;

(iii)

give and reflect a true and fair view of the trading transactions and of the financial and contractual position of the Seller and of its Assets and liabilities in relation to the Platform; and

(iv)

have been prepared in accordance with the generally accepted accounting principles and practices (in the relevant jurisdiction).

9.

Intellectual Property

(a)

Details of the Seller Intellectual Property Rights are set out in Schedule 2 (Owned Rights). In respect of all Owned Rights:

(i)

all registration, application and other fees due for payment have been paid in full by the Seller;

(ii)

they are owned solely by the Seller and, at Completion, will be free of all Encumbrances;

(iii)

no person other than the Seller has any right to use those Owned Rights;

(iv)

so far as the Seller is aware, there has been no unauthorised use by another person of the Owned Rights;

(v)

so far as the Seller is aware, nothing has been done or omitted to be done by the Seller and no other circumstance exists that may affect the validity or ownership of the Owned Rights; and

(vi)

the Seller has not dealt with or granted to any person any rights in respect of any Owned Rights, including under a licence granted by the Seller.

(b)

The Seller has not licensed any of the Seller Intellectual Property Rights and has not assigned or in any way disposed of any right, title or interest in the Seller Intellectual Property Rights except pursuant to any contract, a copy of which has been provided to the Buyer prior to execution of this agreement.

(c)

Neither the carrying on of the Platform, nor the use of the Seller Intellectual Property Rights in the Platform, nor the entry into or performance by the Seller of this document:

(i)

infringes or is alleged to infringe the Intellectual Property Rights of any third party; or

(ii)

is or is alleged to be in breach of any obligation of confidence owed to any third party.

(d)

There has not been:

(i)

any challenge to the Seller’s right, title and interest in and to, or right to use, the Seller Intellectual Property Rights in the jurisdictions in which they are used by the Seller;

(ii)

any infringement of the Seller Intellectual Property Rights; nor

(iii)

any other act or omission which may affect the validity or enforceability of the Seller Intellectual Property Rights.

(e)

The Seller Intellectual Property Rights are valid and enforceable in the jurisdictions in which they are used by the Seller.

(f)

The Seller does not, in the conduct of the Platform, infringe or wrongfully use any Platform names, licences, copyrights, patents, trade marks, service marks, trade names, designs, and similar industrial, commercial or intellectual property (whether registered or not and whether protected by statute or not and including formulae, recipes and know-how) in the conduct of the Platform.

(g)

No disclosure has been made to any person of any industrial know-how or any financial or trade secret of the Seller in connection with the Platform to a person (other than the Buyer) except as required by law.

(h)

There are no royalty, licence or any other fees payable in connection with the Platform or in relation to the conduct of the Platform.

(i)

The Platform's architecture is designed to accommodate the addition of new analysis capabilities, data import functionalities and integration with additional data sources without requiring fundamental restructuring of the core Platform components.

(j)

all Third Party Components are properly licensed, transferable to the Buyer and compliant with all applicable open-source obligations.

10.

Compliance with law and absence of litigation

(a)

there are no Claims in respect of the Platform or any of the Assets and there are no Claims relating to the Platform or the Assets which may give rise to litigation;

(b)

there is no unsatisfied judgment, order, arbitral award or decision of any court, tribunal or arbitrator against the Seller or any of the Assets and there is no outstanding Claim to which the Seller is party pending or threatened against the Seller in respect of the Platform or the Assets;

(c)

the Seller is not a party to any contract, agreement, arrangement or understanding which is in breach of any applicable trade practices legislation in relation to the Platform nor does the Seller engage in any conduct or practice which is in breach of that legislation; and

(d)

the Seller holds all necessary or desirable licences (including statutory licences) and consents, permissions, authorisations and permits for the proper carrying on of the Platform in all its aspects.

11.

Data Protection

(a)

The Seller complies with all applicable laws, guidelines and industry standards relating to the processing of personal data and privacy (Data Protection Laws) in the conduct of the Platform.

(b)

The Seller has in place and operates adequate procedures to ensure the Platform's continued compliance with Data Protection Laws.

(c)

In the last three years, the Seller has not received any notices or any communications from any person:

(i)

alleging non-compliance with any Data Protection Laws; or

(ii)

complaining about its use of personal data, and so far as the Seller is aware, there are no circumstances likely to give rise to any such notices or communications.

(d)

All Platform Records comprising information and records and personal data in relation to users or clients and potential users or clients of the Platform has been obtained in accordance with Data Protection Laws and the Seller is entitled to use, transfer and grant rights in respect of the use of, such data.

12.

Confidential Information

(a)

The Seller has not at any time (save in the ordinary course of Platform, in connection with the transactions contemplated by this agreement, or subject to an obligation of confidentiality or to the professional advisers of the Seller) disclosed to any person other than the Purchaser:

(i)

any of the secret or confidential information or property of the Seller in relation to the Platform, including (without limitation) financial information, plans, statistics, documents, files, recipes, marketing information, records and papers, material to the operation of the Platform; or

(ii)

any secret or confidential information material to the Seller's customers, clients, employees and agents or to any other person who has or has had any dealings with it.

(b)

So far as the Seller is aware, there has been no actual or alleged misuse by any person of any of the secret or confidential information or property of the Seller in relation to the Platform or the Assets.

13.

Future Dealings

12.

Portal Implementation Work means all development work, customizations, configurations, and implementations performed by the Seller specifically for the portal instance of the Platform, including but not limited to:

(a)

custom user interface designs and implementations;

(b)

specific database schemas and data models;

(c)

customized workflows and business logic;

(d)

portal-specific integrations and configurations;

(e)

documentation specific to the portal implementation;

(f)

any other development work performed specifically for the portal instance; and

(g)

all associated intellectual property rights in the above.

13.

Backlink Services

(a)

The Seller warrants that:

14.

Platform and Core Systems

(a)

The Seller warrants that:

15.

All warranties in this Schedule are qualified by and subject to:

(a)

The Buyer's obligation to:

(ii)

Implement proper disclaimers and warnings

(iii)

Ensure proper data protection and privacy measures

(iv)

Follow provided documentation and guidelines

(b)

The understanding that the Buyer assumes full responsibility and liability for:

(i)

Implementation decisions

(ii)

Regulatory compliance

(iii)

Medical and healthcare compliance

(iv)

Data protection

(v)

System modifications

(vi)

Integration decisions

(c)

The limitation that warranties apply only to:

(i)

Newly created Development Work

(ii)

Specified deliverables

(iii)

Documentation provided

(d)

The explicit exclusion of liability for:

(i)

Buyer modifications

(ii)

Implementation decisions

(iii)

Regulatory compliance

(iv)

Medical outcomes

(v)

Data protection issues

16.

Supplement Recommendations

(a)

The Buyer acknowledges and agrees that:

(i)

it is solely responsible for validating all supplement recommendations;

(ii)

it bears full responsibility for drug interaction checking and monitoring;

(iii)

it is responsible for ensuring dosage recommendations comply with safety guidelines;

(iv)

it must maintain and update supplement information;

(v)

it is responsible for validating recommendation algorithms with qualified professionals.

17.

Medical Disclaimers and Compliance

(a)

The Buyer acknowledges and agrees that:

(i)

it is solely responsible for implementing and maintaining medical disclaimers;

(ii)

it must ensure the system indicates it does not provide medical advice;

(iii)

it is responsible for maintaining appropriate warning language;

(iv)

it bears full responsibility for healthcare information regulation compliance;

(v)

it must obtain qualified legal review of disclaimer language.

1.

Core Platform Components

(a)

Platform architecture and frameworks

(b)

Data processing pipelines

(c)

Security implementations

(d)

API frameworks

(e)

User authentication systems

2.

LIMS Integration Systems

(a)

Laboratory data standardization protocols

(b)

Sample tracking frameworks

(c)

Quality control systems

(d)

Results processing engines

(e)

Laboratory workflow optimizations

3.

AI Interpretation Engine

(a)

Machine learning models

(b)

Training datasets

(c)

Variant interpretation algorithms

(d)

Risk assessment systems

(e)

Continuous learning frameworks

4.

Supplement Systems

(a)

Recommendation engines

(b)

Interaction databases

(c)

Dosage calculators

(d)

Safety check systems

(e)

Affiliate integration frameworks

5.

Pregnancy/IVF Module

(a)

Pregnancy analysis rules

(b)

IVF protocol systems

(c)

Timing engines

(d)

Provider reporting tools

(e)

Risk assessment models

6.

Documentation

(a)

Technical specifications

(b)

API documentation

(c)

System architectures

(d)

Database schemas

(e)

Integration guides

7.

Source Code

(a)

Core platform code

(b)

Custom components

(c)

Integration modules

(d)

Testing frameworks

(e)

Deployment configurations

8.

AI Variant Curator

(a)

Rules Engine Components

(i)

Clinical guideline implementation frameworks

(ii)

Compliance validation systems

(iii)

Best-practice verification modules

(iv)

Structured classification pipelines

(v)

Audit trail generators

(b)

LLM Components

(i)

LLM integration frameworks

(ii)

Scientific database connectors

(iii)

Literature parsing engines

(iv)

Summary generation systems

(v)

Context extraction modules

(c)

Integration Layer

(i)

Hybrid decision reconciliation system

(ii)

Combined output formatter

(iii)

Audit trail integrator

(iv)

Self-hosting configurations

(v)

HIPAA compliance implementations