Expert Group on the Application of the 3Rs in Regulatory Testing of Medicinal Products (JEG 3Rs)
Owner/Developer: European Medicines Agency (EMA)
| Country: | United Kingdom |
|---|---|
| Languages: | English |
| Url: | https://www.ema.europa.eu/en/human-regulatory-overview/research-development/ethical-use-animals-medicine-testing |
| Description: |
The Joint Committee for Medicinal Products for Veterinary Use/Committee for Medicinal Products for Human Use Ad-hoc Expert Group on the Application of the 3Rs in Regulatory Testing of Medicinal Products (JEG 3Rs) provided advice and recommendations to the Committee for Medicinal Products for Veterinary Use (CVMP) and Committee for Medicinal Products for Human Use (CHMP) on all matters relating to the use of animals and the application of the '3 R' principles (replacement, reduction and refinement) in the testing of medicines for regulatory purposes. It is now part of the European Medicines Agency's 3Rs Working Party (3RsWP). Empl et al. (2026): 3Rs at The European Medicines Agency: Past and future activities |
| Category: | Experts |
| Channel: | Website |
| Audience: | Industry - Regulators |
| User access: | Open access |
| Relevance: | Replacement - Reduction - Refinement |
| Purpose: | Documentation and information - Regulatory testing |
| Legislative framework: | Medicines legislation |
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