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A clinical protocol defines the plan for a clinical trial, detailing every aspect of how the study w...
The Good Clinical Practice (GCP) course is designed to prepare research staff in the conduct of clin...
Good clinical practices-drug discovery
GCP guidelines for clinical research
Good Clinical Practices and Investigator responsibilities
GCP is a set of guidelines for how clinical trials should be carried out. It ensures that the data...
4. Unit-IV:- Clinical Trials. B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY SC...
Good Clinical Practices for drug discovery and development
Good clinical practice guidelines
Slides prepared for IIUM GCP Workshop
Informed consent process a prerequisite in any clinical trial study as an understanding between the...
this slide tells about schedule Y, Good Clinical Practice, CDSCO, Ethics committee, consent form, Se...
Quality Assurance and Quality Control in Clinical Research
for the better understanding of the student
Describes in detail definition, purpose, participants and goal of good clinical practices (GCP). Giv...
Turacoz Skill Development Program provides medical writing training on various types of regulatory d...
ICH
ICH GUIDELINES OF EFFICACY AND MULTIDISCIPLINARY
This presentation gives an overview on Clinical trial Protocol development
Sop writing for research sites
baik
the clinical research team and their Roles & responsibility.
The term ‘’essential documents’’ refers to the documents which, according to the ICH-GCP Gui...