Sentence examples for approval of trials from inspiring English sources

The approval of trials by legitimate government authorities, with limited consultation or engagement with other stakeholders in the host community, was severely criticized by a wide range of stakeholders.

Those faced with granting ethical approval of trials of contraception in children <16 years of age need to be satisfied that such trials are both scientifically justified and lawful and that appropriate mechanisms to respect confidentiality and provide safeguards for participants are in place.

A gap of at least 4 weeks in delamanid treatment existed between Trial 204 and Trail 208, resulting from the Trial 204 design and the timing of local regulatory and ethics approval of Trial 208; all patients continued with OBR throughout this period.

It would probably adopt a proposal made by the AMA that registration in a central database be a requirement for the approval of human trials, as well as introducing new requirements to include trial results in the database.The industry disputes the need for this.

Therefore, major efforts should be made to reduce and standardize procedures concerning the approval of clinical trials, also focusing on administrative procedures, because time to trial activation is critical for clinical research.

What we are likely to get, if Bush is wise enough to ask for it, is Congressional approval of overseas trials of terrorist leaders by military courts adhering to basic standards of U.S. military justice.

This poses a significant hurdle for AO drug development as drug developers will be unable to validate the efficacy of AO targeting human dystrophin exon in animal models, which is generally considered to be essential for regulatory approval of clinic trials.

Other challenges in Brazil and South Africa were primarily related to delays in approval of clinical trials, which was perceived to detract from a major competitive advantage possessed by these countries.

To assist in the development of preclinical and clinical tools, NIAID provides standardized reagents and vaccine and drug testing services in animal models of TB, and also provides non-clinical development and manufacturing resources to help complete data packages needed for regulatory approval of clinical trials.

This is partly due to the lack of understanding and working knowledge in quantitative pharmacology and pharmacometrics by sponsors, regulatory agencies and investigators (e.g. paediatricians, statisticians, research nurses) who are responsible for the planning, design and/or approval of clinical trials.

Additionally, with the approval of the trial DSMB, we used actual trial data on HIV prevalence and the proportion who receive a CD4 count to refine our sample size requirements.