Sentence examples for trials material from inspiring English sources

Exact(2)

Results indicate that accuracy profiles are similar in the two conditions; however, the patterns of data measuring inhibitory control, i.e., percentage of intrusion errors, are opposite in the case of verbal (intrusions decreased in more complex trials) and visuo-spatial (intrusions increased in more complex trials) material.

The Cancer Research UK Formulation Unit at the University of Strathclyde is already licensed to manufacture clinical trials material, and the Biotherapeutics Development Unit at the Cancer Research UK London Research Institute (Clare Hall) will also be licensed before the EU legislation is implemented.

Similar(57)

Throughout day 1, subjects completed 7 runs that each contained 16 retrieval trials (Materials and methods, Procedure).

TU wrote the study protocol and other clinical trials materials, supervised by RJB, secured regulatory approvals, set up the study and wrote the first draft of the manuscript.

Doar, which provides consulting services on courtroom design, also offers software that helps lawyers prepare and manage trial material and do jury research.

Gradually 3D Disco took shape through trialing material in their hometown of Newcastle's Wax On night, and progressed to performing in Trafalgar Square with Calvin Harris.

As well as trialling material for his forthcoming UK tour over the first few days of the fringe, Harry Hill is also showcasing his artistic talents in his first public exhibition of paintings and sculptures, My Hobby, which opened on Friday at White Stuff and runs until 2 September.

A key recommendation for future studies is conduct consistent with Good Clinical Practice (GCP), including use of Good Manufacturing Practice GMPP) quality clinical trial material.

In addition, these data could also be used to justify the retest period for clinical trial material and to justify lean post-approval protocols.

We emphasize the importance of incorporating biospecimen collection into trial design, and wording patient consents to allow post hoc analysis of trial material as new data become available.

If the trial is closed prematurely, the trial material such as completed, partially completed, and blank CRFs will be returned to the coordinating investigator.

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