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4. Unit-IV:- Clinical Trials. B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY SC...
From history and with case studies
Good Clinical Practice (GCP) guidelines are a set of international ethical and scientific standards ...
In any work or process documents that are needed before initiation, Between or generally the end of ...
stake holders in clinical trail
Clinical research associate responsebility
The ppt gives a basic information about ICH-GCP, how it originated , what led to the formation of IC...
This PPT give information about Institutional Human Ethics Committee
ICH E 6 good clinical practice (GCP)
An overview of ICH-GCP guidelines of clinical trials. Good clinical practice (GCP): a standard for t...
Embark on a comprehensive journey into the dynamic and critical realm of Clinical Research. This pre...
INVESTIGATOR'S BROCHURE as per ICH E6 (ICH GCP)
Informed consent is a process in which a patient or research participant is provided with informatio...
An informed consent form is a document that is provided to prospective participants in a research st...
ICH GCP guidelines for mpharmacy 2nd sem 204T subject. topic include the brief description regarding...
Good clinical practice guidelines
Pharmacovigilance
Informed consent form
inform consent form before participate in clinical trials.for purpose of understanding the nature of...
baik
Informed consent process a prerequisite in any clinical trial study as an understanding between the...
Good Clinical Practices
Good Clinical Practices for drug discovery and development
Research Code of ethics Ethical principles code of professional conduct Ethics committee
