Found 127 presentations matching your search
Describes in detail definition, purpose, participants and goal of good clinical practices (GCP). Giv...
ICH E 6 good clinical practice (GCP)
The term ‘’essential documents’’ refers to the documents which, according to the ICH-GCP Gui...
4. Unit-IV:- Clinical Trials. B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY SC...
Good clinical practice guidelines
ICH
this slide tells about schedule Y, Good Clinical Practice, CDSCO, Ethics committee, consent form, Se...
ICH GUIDELINES OF EFFICACY AND MULTIDISCIPLINARY
This presentation gives an overview on Clinical trial Protocol development
for the better understanding of the student
Presentation on ICH-GCP guideline.
Turacoz Skill Development Program provides medical writing training on various types of regulatory d...
In these slides you can get the information of clinical trials which have four phase I,II,III, IV. b...
Good Clinical Practice Principle of ICH GCP Institutional Review Board (IRB)/IEC Informed Consent
the clinical research team and their Roles & responsibility.
ICH guidelines
*RA or government affairs, is a profession involved in monitoring and regulating the development, m...
Investigator roles
investigator purpose of investigator role of investigator in study
Quality Assurance and Quality Control in Clinical Research
This presentation based on the Informed Consent Process and Procedure in Regulatory Affairs.
NARGUND COLLEGE OF PHARMACY
Main regulatory agencies involved in Clinical Trial in nutshell
Contents Guidelines for Preparation of Documentation Clinical Study Reports Clinical Trial Monitorin...
