Property:DocType
From GxPlex
Document type (Legal act, Regulation, Guideline, …).
U
Official recommendation +
USA FDA Guidance for Industry - Oversight of Clinical Investigations — A Risk-Based Approach to Monitoring Aug-2013 +
Official recommendation +
USA FDA Guidance for Industry Investigator Responsibilities — Protecting the Rights, Safety, and Welfare of Study Subjects Oct-2009 +
Official recommendation +
USA FDA INFORMATION SHEET - Recruiting Study Subjects, Guidance for Institutional Review Boards and Clinical Investigators Jan-1998 +
Official recommendation +
Official recommendation +
Official recommendation +
Official recommendation +
A
U
USA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024 +
Other +
W
Other +
N
E
Preamble of legal act +
Preamble of legal act +
Preamble of legal act +
A
Regulatory requirement +
D
Regulatory requirement +
