Pages that link to "Template:DocumentData"

The following pages link to Template:DocumentData:

Displaying 50 items.

• Document:GBR The Electronic Identification and Trust Services for Electronic Transactions (Amendment etc.) (EU Exit) Regulations 2019 23-Jan-2019 (transclusion) (← links)
• Document:GBR The Human Medicines Regulations 2012 01-Jan-2025 (transclusion) (← links)
• Document:GBR The Medical Devices Regulations 2002 11-Feb-2021 (transclusion) (← links)
• Document:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 (transclusion) (← links)
• Document:GBR UK GDPR - United Kingdom General Data Protection Regulation 31-Dec-2020 (transclusion) (← links)
• Document:USA 21 CFR Part 11 09-Apr-2025 (transclusion) (← links)
• Document:USA 21 CFR Part 312 09-Apr-2025 (transclusion) (← links)
• Document:USA 21 CFR Part 314 09-Apr-2025 (transclusion) (← links)
• Document:USA 21 CFR Part 320 09-Apr-2025 (transclusion) (← links)
• Document:USA 21 CFR Part 50 09-Apr-2025 (transclusion) (← links)
• Document:USA 21 CFR Part 54 09-Apr-2025 (transclusion) (← links)
• Document:USA 21 CFR Part 56 09-Apr-2025 (transclusion) (← links)
• Document:USA 21 CFR Part 809 06-May-2024 (transclusion) (← links)
• Document:USA 21 CFR Part 812 09-Apr-2025 (transclusion) (← links)
• Document:USA 42 CFR Part 11 09-Apr-2025 (transclusion) (← links)
• Document:USA 45 CFR Part 160 09-Apr-2025 (transclusion) (← links)
• Document:USA 45 CFR Part 46 09-Apr-2025 (transclusion) (← links)
• Document:USA Acceptance of Clinical Data to Support Medical Device Applications and Submissions Frequently Asked Questions - Guidance for Industry and Food and Drug Administration Staff 21-Feb-2018 (transclusion) (← links)
• Document:USA CTCAE - Common Terminology Criteria for Adverse Events v5.0 (2017) (transclusion) (← links)
• Document:USA Expedited Review: Categories of Research that may be Reviewed Through an Expedited Review Procedure 1998 (transclusion) (← links)
• Document:USA FD&C Act - Federal Food, Drug, and Cosmetic Act 30-Sep-2023 (transclusion) (← links)
• Document:USA FDA - E6(R2) Good Clinical Practice: Integrated Addendum to ICH E6(R1): Guidance for Industry March 2018 (transclusion) (← links)
• Document:USA FDA - HUMAN DRUG CGMP NOTES Volume 8, Number 3 (transclusion) (← links)
• Document:USA FDA Guidance for Clinical Investigators, Sponsors, and IRBs Adverse Event Reporting to IRBs — Improving Human Subject Protection Jan-2009 (transclusion) (← links)
• Document:USA FDA Guidance for Industry - Computerized Systems Used in Clinical Investigations May-2007 (transclusion) (← links)
• Document:USA FDA Guidance for Industry - Computerized Systems Used in Clinical Trials 13-Apr-2015 (transclusion) (← links)
• Document:USA FDA Guidance for Industry - Conduct of Clinical Trials of Medical Products During the COVID-19 Public Health Emergency Mar-2020 (transclusion) (← links)
• Document:USA FDA Guidance for Industry - Electronic Source Data in Clinical Investigations Sep-2013 (transclusion) (← links)
• Document:USA FDA Guidance for Industry - Oversight of Clinical Investigations — A Risk-Based Approach to Monitoring Aug-2013 (transclusion) (← links)
• Document:USA FDA Guidance for Industry Investigator Responsibilities — Protecting the Rights, Safety, and Welfare of Study Subjects Oct-2009 (transclusion) (← links)
• Document:USA FDA INFORMATION SHEET - Recruiting Study Subjects, Guidance for Institutional Review Boards and Clinical Investigators Jan-1998 (transclusion) (← links)
• Document:USA NIH - Glossary 27-May-2025 (transclusion) (← links)
• Document:USA FDA Information - Observations and citations 20-Mar-2024 (transclusion) (← links)
• Document:USA Informed Consent - FDA Guidance for IRBs, Clinical Investigators, and Sponsors Aug-2023 (transclusion) (← links)
• Document:USA NCI GUIDELINES FOR INVESTIGATORS: ADVERSE EVENT REPORTING REQUIREMENTS FOR DCTD (CTEP AND CIP) INDs AND IDEs 30-Aug-2024 (transclusion) (← links)
• Document:USA NIH - SCORE Manual N.A. (transclusion) (← links)
• Document:USA NIH - SCORE Manual: Appendix Source Documents Requirements Rev 01 16-Aug-2025 (transclusion) (← links)
• Document:USA Recognized Consensus Standards N.A. (transclusion) (← links)
• Document:USA Recognized Consensus Standards - ISO 14155 21-Dec-2020 (transclusion) (← links)
• Document:USA U.S. Code Title 21 30-Sep-2023 (transclusion) (← links)
• Document:CIOMS CIOMS - International Ethical Guidelines for Biomedical Research Involving Human Subjects 2016 (transclusion) (← links)
• Document:CIOMS CIOMS - International Ethical Guidelines for Health-related Research Involving Humans 2016 (transclusion) (← links)
• Document:CIOMS CIOMS Publications - (transclusion) (← links)
• Document:ICH ICH E11 Guideline R1 (2017) (transclusion) (← links)
• Document:ICH ICH E19 Guideline 2022 (transclusion) (← links)
• Document:ICH ICH E21 Concept paper 2023 (transclusion) (← links)
• Document:ICH ICH E2A Guideline 1994 (transclusion) (← links)
• Document:ICH ICH E2F Guideline 2010 (transclusion) (← links)
• Document:ICH ICH E3 Guideline 1995 (transclusion) (← links)
• Document:ICH ICH E6 Guideline R3 (2025) (transclusion) (← links)