At its core, convenient clinical p...

At its core, convenient clinical practice (GCP) is a risk of broad regulatory requirements, standards, and recommendations that apply to thousands of highly specific tasks, processe and parts in the conduct of clinical research. Given the disparity between the specificity of clinical trial processe and tasks and the general GCP requirements and standards in a less degree than which they occur, it is not surprising that interpreting and implementing GCP standards continues to existing challenges to the pharmaceutical, bio-technology, and medical device industries.

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