Pages that link to "Glossary:TAG-00003-Adv-cht"
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The following pages link to Glossary:TAG-00003-Adv-cht:
Displaying 20 items.
- Glossary (â links)
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 Article 2 Paragraph 2 No. 1 (â links)
- Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 2 clinical trial (â links)
- Reference:GBR Directive 2001/20/EC 04-Apr-2001 Article 2 (a) (â links)
- Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.32 - Life-threatening Adverse event (â links)
- Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 2 adverse event adverse reaction (â links)
- Reference:ICH ICH E6 Guideline R3 (2025) GLOSSARY - Adverse Drug Reaction (ADR) (â links)
- Reference:ICH ICH E2A Guideline 1994 II B. Serious Adverse Event or Adverse Drug Reaction (â links)
- Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 Glossary - adverse reaction (â links)
- Reference:EU 2011/C 172/01 - CT-3 11-Jun-2011 Section 7 7.3.2 (â links)
- Reference:GBR Directive 2001/20/EC 04-Apr-2001 Article 2 (n) (â links)
- Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.32 - Suspected adverse reaction (â links)
- Reference:ICH ICH E2A Guideline 1994 II A. 3. (â links)
- Reference:ICH ICH E2A Guideline 1994 III A. 1. (â links)
- Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 2 unexpected adverse reaction (â links)
- Reference:GBR Directive 2001/20/EC 04-Apr-2001 Article 2 (p) (â links)
- Reference:USA 21 CFR Part 312 09-Apr-2025 § 312.32 - Unexpected adverse event (â links)
- Reference:ICH ICH E2A Guideline 1994 III B. - III C. (â links)
- Reference:WHO WHO - Guidelines for GCP for trials on pharmaceutical products* 1995 7.2 - Sponsor (â links)
- Reference:EU Regulation (EU) 536/2014 - clinical trials 05-Dec-2022 ANNEX III Section 2.1 (â links)