Study reference manual clinical trial

 

 

STUDY REFERENCE MANUAL CLINICAL TRIAL >> DOWNLOAD LINK

 

STUDY REFERENCE MANUAL CLINICAL TRIAL >> READ ONLINE

 

 

 

 

 

 

 

 

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4, a key responsibility of an investigator is to maintain trial-related documents which permit evaluation of the conduct of a trial and the quality of the dataThese documents may be referred to in the MOP as “dynamic references. In multi-site clinical studies, a Steering Committee, comprised of the principal Implementation of NCCIH Policies for Clinical Studies Procedures (MOP) template for principal investigators (PIs) of multisite clinical trials.

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