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- Document:USA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024 + (USA)
- Document:USA NIH - SCORE Manual N.A. + (USA)
- Document:USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025 + (USA)
- Document:USA Recognized Consensus Standards N.A. + (USA)
- Document:USA Recognized Consensus Standards - ISO 14155 21-Dec-2020 + (USA)
- Document:USA U.S. Code Title 21 30-Sep-2023 + (USA)
- Document:USA WARNING LETTER - Purolea Cosmetics Lab MARCS-CMS 722591 46114 + (USA)
- Document:USA 21 CFR Part 312 09-Apr-2025 + (USA)
- Document:WHO WHO - EXPERT COMMITTEE ON SPECIFICATIONS FOR PHARMACEUTICAL PREPARATIONS Forty-fifth report + (WHO)
- Document:WHO WHO - Guidance for best practices for clinical trials 2024 + (WHO)
- Document:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 + (WHO)
- Document:WHO WHO - HANDBOOK FOR GOOD CLINICAL RESEARCH PRACTICE (GCP) 2005 + (WHO)
- Document:WHO WHO - ICD 11 + (WHO)
- Document:WHO World Health Organization - + (WHO)
- Document:WHO WHO Good Practices for Clinical Trial Design and Implementation 04-May-2026 + (WHO)
