Sentence examples for trial documentation from inspiring English sources

Competent authorities and sponsor authorised persons (auditor) may request access to all source documents, CRF and other trial documentation in case of an inspection or audit.

To investigate the technical feasibility of a study dashboard for monitoring the progress of patient recruitment and trial documentation, we set out to develop a propositional prototype in the form of a separate software module.

Please note: The Clinical Trial Agreements team has the authority to execute (i.e., sign) clinical trial documentation (e.g., clinical trial agreements and confidential disclosure agreements (CDAs) that legally binds the University.

Again, the details of the dressings used will be recorded in the trial documentation.

The patient will then receive a trial ID that will be used on all trial documentation.

13 Following wound closure, the tourniquet will be released and the 'tourniquet-down time' noted on the trial documentation.

Today, I translate a lot of medical materials--product information, user manuals, patient information, and clinical trial documentation--as well as more scientific items, such as research papers, abstracts, dissertations, and patents.

But in court filings, plaintiff lawyers say defendant companies benefit from special rules that are more restrictive than the general rules of procedure in New York courts, including strict limits on the number of plaintiffs that can be included in a single trial and requirements for extensive pre-trial documentation of claims.

Therefore, further trial related documentation will be performed at 10 and 15 years post treatment.

We examined associations between whether studies had any authors from a low or middle income country (yes or no) and the following variables: year of publication, cancer site, funding type, multi- versus single-centre participation, use of placebo, type of treatment, treatment aim, type of randomized trial, ethics documentation, and whether the study mentioned informed consent.

This experience should serve to improve the design of future trials, their documentation and preservation of patient data for future analyses.