No Additional Research Clause Samples
The "No Additional Research" clause establishes that the party providing services or information is not required to conduct any research beyond what is already agreed upon or within the scope of the contract. In practice, this means the provider is only responsible for using existing knowledge, resources, or materials, and is not obligated to seek out new data, perform extra investigations, or generate new reports unless specifically requested and agreed to. This clause helps prevent scope creep and unexpected costs by clearly limiting the provider's obligations to what was initially contemplated.
No Additional Research. No additional research may be conducted on Trial Subjects during the conduct of the Trial, unless it is approved by Sponsor and documented as a companion protocol or an Amendment to the original Protocol. Such prohibited research activities include analyses of biological samples from Trial Subjects for any non-therapeutic purpose.
No Additional Research. No additional research may be conducted on Study Subjects (as defined in Section 4, Subject Enrollment) during the conduct of the Study or on biological samples collected during the conduct of the Study unless it is approved by Pfizer and documented as an Amendment to the Protocol or made subject to mutually agreeable terms otherwise documented by the parties.
No Additional Research. No additional research may be conducted on Study Subjects (as defined in Section 4, Subject Enrollment) during the conduct of the Study or on biological samples collected during the conduct of the Study unless it is approved by Pfizer and documented as an Amendment to the Protocol or made subject to mutually agreeable terms otherwise documented by the parties. 3.2 Žádný dodatečný výzkum. Na subjektech Studie (definovaných v článku 4, Zařazení subjektů) nebo na biologických vzorcích odebraných v průběhu Studie nesmí být v průběhu Studie prováděn žádný dodatečný výzkum, pokud to není schváleno společností Pfizer a zdokumentováno Dodatkem k Protokolu nebo učiněno za vzájemně přijatelných podmínek, zaznamenaných stranami jiným způsobem.
No Additional Research. No additional research may be conducted on Trial Subjects during the conduct of the Trial, unless it is approved by Sponsor and documented as a companion protocol or an Amendment to the original Protocol. Such prohibited research activities include analyses of biological samples from Trial Subjects for any non-therapeutic purpose. Zákaz dalšího výzkumu Během provádění klinického hodnocení nesmí být u subjektů klinického hodnocení prováděn žádný další výzkum, dokud to neschválí zadavatel a výzkum není zdokumentován jako přidružený protokol nebo dodatek původního protokolu. Tyto zakázané výzkumné činnosti zahrnují analýzu biologických vzorků od subjektů klinického hodnocení pro jiné než léčebné účely.
No Additional Research. No additional research may be conducted on Human Subjects during the conduct of the Trial or on biological samples collected during the conduct of the Trial unless it is approved by SPONSOR and the responsible IRB/IEC and documented as an Amendment to the Protocol or made subject to mutually agreeable terms otherwise documented by the parties.
No Additional Research. No additional research will be conducted on Study subjects during the conduct of the Study unless it is approved in writing by Sponsor. Such prohibited research activities include, but are not limited to, analysis of biological samples from Study subjects for any non-therapeutic purpose.
No Additional Research. No additional research may be conducted on Study Subjects
No Additional Research. Institution confirms that no additional research will be conducted on Study Subjects during the conduct of the Study, unless it is approved by Sponsor and documented as a companion protocol or an Amendment to the original Protocol. Such prohibited research activities include analyses of biological samples from Study Subjects for any non-therapeutic purpose. dcérske spoločnosti musia dodržiavať ustanovenia (i) Protikorupčného zákona Spojeného kráľovstva z r. 2010 (Protikorupčný zákon); (ii) Zákona o zahraničných korupčných praktikách Spojených štátov amerických z r. 1977 (FCPA) a (iii) všetky ďalšie platné protikorupčné právne predpisy.
No Additional Research. No additional research may be conducted on Study subjects during the conduct of the Study or on biological samples collected during the conduct of the Study unless it is approved by Sponsor and documented as an Amendment to the Protocol or made subject to mutually agreeable terms otherwise documented by the parties. 26. Zákaz dalšího výzkumu. Během provádění studie nesmí být se subjekty studie nebo s biologickými vzorky odebranými během provádění studie realizován žádný další výzkum, pokud to nebylo schváleno Zadavatelem a zaznamenáno formou dodatku k protokolu nebo pokud se to nestalo předmětem vzájemně přijatelných podmínek zaznamenaných smluvními stranami jiným způsobem.
No Additional Research. No ▇▇▇▇▇▇▇▇▇▇ ▇ ▇▇▇▇ ▇▇▇▇▇▇▇▇▇ ▇▇▇▇▇▇. Na subjektech research may be conducted on Study Subjects (as defined in Section 4, Subject Enrollment) during the conduct of the Study or on biological samples collected during the conduct of the Study unless it is approved by Pfizer and documented as an Amendment to the Protocol or made subject to mutually agreeable terms otherwise documented by the parties. Studie (definovaných ▇ ▇▇▇▇▇▇ ▇, ▇▇▇▇▇▇▇▇ subjektů) nebo na biologických vzorcích odebraných v průběhu Studie nesmí být v průběhu Studie prováděn žádný dodatečný výzkum, pokud to není schváleno společností Pfizer a zdokumentováno dodatkem protokolu nebo učiněno za vzájemně přijatelných podmínek zaznamenaných stranami jiným způsobem.