Technical Monitor definition

Technical Monitor. The CONTRACTOR designated individual(s) representing the end user of the Order. May be the same individual as the ‘hiring manager’ requiring services or an intermediary managing the work outlined in the Order. This person is necessary for the successful performance of the Order and is accountable for stewardship of the Subcontractor’s technical performance.
Technical Monitor means an advisor to the Contracting Officer on the technical performance of the contract.
Technical Monitor. SHamel Status: Ongoing

Examples of Technical Monitor in a sentence

  • If the Subcontractor is requested to work overtime due to an unplanned or emergency requirement, the Subcontractor shall notify the Subcontract Administrator and Technical Monitor (defined as the site contact in charge of the work specified and authorized in the Order), via email, within two (2) business days of the overtime performed.

  • The Consultant shall notify the FHI 360 Technical Monitor in writing when costs incurred under this contract, will exceed 75% of the total amount so far allotted to the contract by FHI 360.

  • The Recipient is expected to implement the project via work plans, which require collaboration with and approval by HUD’s Government Technical Monitor (“GTM”) and HUD’s Government Technical Representative (“GTR”).

  • The Government may designate the M&O Contractor to be the Technical Monitor for any right, duty or interest in this Contract.

  • Acceptance of all items and/or services under this agreement shall be made by the Technical Monitor or his/her designee specified in Part I of this Agreement.

  • Inspection and acceptance of contractor performance will be made by the Contracting Officer Representative (COR) and associated Government Technical Monitor (GTM).

  • If the Town would like reports delivered a different way, K+A is flexible in regards to how test results can be reported.

  • The revised scope of work as proposed by ▇▇▇▇▇ Pharmaceuticals has been reviewed and approved by the Technical Monitor on 16 February 2005 and will become effective upon the date of this modification.

  • The Contractor agrees to fully cooperate with the M&O Contractor, other contractors, and Government employees, and carefully coordinate its own work The Government may designate the M&O Contractor to be the Technical Monitor for any right, duty or interest in this Contract.

  • The Procurement Executive may direct a contracting officer to revoke the appointment memorandum of a Contracting Officer’s Representative or Government Technical Monitor who makes an unauthorized commitment.


More Definitions of Technical Monitor

Technical Monitor. HReynolds Status: Complete Comparing the current standard of care (infants get their NVP dose at the facility within 72 hours) with the new strategy (to give the dose to the mothers to administer at home), the study seeks to measure the proportion of HIV+ pregnant women in antenatal care (ANC) who received the infant take home NVP dose and the proportion of women who give the infant dose. To implement the study, we are working in sites supported by FHI, and providers systematically fill and distribute the infant dose to all women greater than or equal to 32 weeks gestation in a subset of facilities. We are collaborating with PATH on this project who has developed packaging material for the infant dose. Another subset of women in matched facilities will serve as the control group. We will follow up women in the training group at home to interview them about their experiences with the infant NVP dose. In the control group, we will also follow up HIV- infected women who attend ANC at greater than or equal to 32 weeks to understand the factors that facilitated them to take their infant for the dose at the facility or not. We will compare the proportion of women whose infants received the NVP dose between the two groups. We will also be able to investigate the factors associated with NVP use or non-use. The major limitation of the study is we rely on women’s reports. This activity was approved for spending and continue as a no-cost extension activity of the CTR through August 31, 2006. • The protocol was prepared, reviewed, and approved by FHI’s PHSC on November 11, 2005. • Data collection instruments were finalized in December 2005. • ▇▇▇▇▇▇▇▇ National Hospital’s Ethical Review Committee approved the study in February 2006. • The consultant was hired in February 2006. • Research assistants were trained during March 2006. • FHI staff traveled to study sites in April 2006 to train providers in infant nevirapine dose filling and distribution. • Data collection and data entry started in March and is expected to end in July 2006.
Technical Monitor. WCastro Status: Ongoing
Technical Monitor. CMorrison Status: Complete The secondary objective of this subproject is to analyze the potential effect of hormonal contraception and pregnancy in the expression of hBDs in the genital tract of women from the Ugandan and Zimbabwean cohort and how this may correlate to protective immunity against HIV at the mucosal level. For the secondary objective, samples will be obtained from three different contraceptive groups:
Technical Monitor. ERaymond Status: Ongoing Considering the public health importance of both progestin-only methods and STIs, clarification of this issue is urgently needed. In addition, the role of herpes simplex virus (HSV) infection in mediating an increased HIV risk associated with depot medroxyprogesterone acetate (DMPA), as suggested in one recent study, needs further evaluation. The best way to provide this clarification would be through a randomized trial. This subproject will support activities aimed at assessing the feasibility of a randomized trial to investigate the effects of DMPA on the incidence of GC and CT and possibly HSV, and if feasible, support the application to other donors for funding to implement the trial. Anticipated activities may include: developing the trial protocol; selecting study sites which will require surveys at multiple locations to assess the feasibility of recruitment and the incidence of GC/CT/HSV in prospective trial populations, and visits to sites that seem promising; and investigating sources of funding for the trial.
Technical Monitor. ▇▇▇▇▇ Status: Ongoing To address this issue, FHI proposes a two-phase study. Phase I will consist of formative research. Interviews with PMTCT clients in 6 sites will assess the priority they place on preventing or delaying a future pregnancy and will explore their interest in receiving FP services under different service delivery configurations e.g. during antenatal care, post-partum visits, immunization and well baby check-ups. Providers and facility supervisors of each of these services will also be interviewed to assess their willingness to take on the added responsibility of providing FP services. Results of data collection will be shared with program managers, who will identify one or two integration interventions that appear to be the most feasible. Phase II will consist of operations research to test the selected interventions. It is anticipated that for each intervention, five matched pairs of PMTCT sites will be identified to participate. At baseline, PMTCT clients consenting to be re-contacted will be interviewed to assess their current contraceptive use. For each of the five matched pairs of PMTCT sites, one site will be randomly assigned to receive the intervention and the other site will continue delivering PMTCT as usual. After a 6-month follow-up period, another cross-section of PMTCT clients will be interviewed. Process data will also be collected to assess the extent to which the intervention was implemented as intended. Finally, the cost of implementing the intervention will be computed to inform decisions about scale-up.
Technical Monitor. JKimani Status: Ongoing International recommendations, country-specific guidelines, and program documents for contraceptive use by people at risk of HIV and HIV-infected, including women on ART changed or strengthened

Related to Technical Monitor

  • Contract Monitor means the Department employee identified in Section 1.6 of the IFB as the Contract Monitor.

  • Technical Documentation means designs, reports, photographs, drawings, plans, specifications, computer software, surveys, calculations and other data, information and material collected, computed, drawn or produced, including computer print-outs.

  • Technical Support Services means the technical support and maintenance Services provided by us according to our then-current technical support policy and procedure listed at ▇▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇ (“Technical Support Policy”) when the Services are purchased.

  • Technical Services means all services that are necessary to carry out individual, scattered site activities including but not limited to: (1) conducting initial inspections, (2) work write-up or project specification development, (3) cost estimate preparation, (4) construction supervision associated with activities that do not require an architect or engineer, (5) lead hazard reduction or lead abatement need determination and oversight, (6) lead hazard reduction or abatement carrying costs, (7) temporary relocation coordination, (8) financing costs such as security agreement preparation and recording or filing fees, (9) processing of individual applications for assistance, (10) income eligibility determination and verification, (11) value determination (new construction) or after rehabilitation value determination (existing structures), and (12) project-specific environmental clearance processes.

  • Market Monitor means the head of the Market Monitoring Unit.