Found 93 presentations matching your search
Good Clinical Practices and Investigator responsibilities
Describes in detail definition, purpose, participants and goal of good clinical practices (GCP). Giv...
Slides prepared for IIUM GCP Workshop
4. Unit-IV:- Clinical Trials. B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY SC...
ICH GUIDELINES OF EFFICACY AND MULTIDISCIPLINARY
ICH
baik
ICH guidelines
INVESTIGATOR'S BROCHURE as per ICH E6 (ICH GCP)
In these slides you can get the information of clinical trials which have four phase I,II,III, IV. b...
Quality Assurance and Quality Control in Clinical Research
the clinical research team and their Roles & responsibility.
ICH Guideline – Q9
inform consent form before participate in clinical trials.for purpose of understanding the nature of...
ICH Guidelines were created by The International Council for Harmonization of Technical Requirements...
Informed consent form
clinical research
what are the Source documents in clinical trial brief in presentation by Kiran Rajput MSc in clinic...
A standard for the design, conduct, performance, monitoring, auditing, recording, analyses and repor...
Good Clinical Practices
This presentation based on the Informed Consent Process and Procedure in Regulatory Affairs.
This presentation gives an overview on Clinical trial Protocol development
A brief discussion on informed consent process and its implementation in clinical trial.
ETHICS IN BIOMEDICAL RESEARCH (Clinical Research).
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