Search Results for "gcp obligations of investigators"

Sponsor responsibilities in Clinical Trial

Sponsor Responsibilities in clinical research as per ICH GCP E6

Healthcare

ROLES AND RESPONSIBILITIES OF sponsor and CRO.pptx

describe about role of sponsor and CRO on clinical trial process

Healthcare

Investigator's Brochure - The Road Map for Investigators

The Investigator's Brochure (IB) is a crucial document in the realm of clinical research and dru...

Healthcare

4. Unit-IV:- Clinical Trials.

4. Unit-IV:- Clinical Trials. B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY SC...

Healthcare

Clinical Trial_3_Fundamentals_Protocol Development.pptx

This presentation gives an overview on Clinical trial Protocol development

Healthcare

Different Types of Regulatory Documents

Turacoz Skill Development Program provides medical writing training on various types of regulatory d...

Healthcare

Clinical trial protocol, ammendments, Protocol deviations and violations

GCP course material

Healthcare

ICH-GCP.pptx

ICH GCP guidelines for mpharmacy 2nd sem 204T subject. topic include the brief description regarding...

Healthcare

Schedule Y by akshdeep sharma

Schedule Y

General

INSTITUTIONAL REVIEW BOARD/INDEPENDENT ETHICS COMMITTEE (IRB/IEC)

regulatory affairs

Business

Informed consent in Clinical Trials

A brief discussion on informed consent process and its implementation in clinical trial.

Healthcare

New Drug Approval Process .pptx

This New Drug Approval Process The new drug approval process is a complex and rigorous process that...

Technology

ICH-GCP_E6_Gudelines_Section 1_History_Principles & Background of GCP.pptx

ICH

General

Declaration of helsinki (Pharmacology SEM-III)

Research Methodology and Biostatistic...Declaration of Helsinki

Healthcare

6 ind

General

Criticism of drug promotional literature(dpl)

HOW TO CRITICALLY APPRAISE A DPL

Technology