Expert Group on the Application of the 3Rs in Regulatory Testing of Medicinal Products (JEG 3Rs)
Owner/Developer: European Medicines Agency (EMA)
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) provides 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.
|Audience:||Industry - Regulators|
|User access:||Open access|
|Relevance:||Replacement - Reduction - Refinement|
|Purpose:||Documentation and information - Regulatory testing|
|Legislative framework:||Medicines legislation|
Did you find what you were looking for?Yes, I found it! No, I did not!
Thanks for your feedback! Please note that we cannot respond unless you supply your email address.
What are you looking for?
Please give us your feedback so we can improve the information on the page. Thank you in advance for your help. Please add your email address if you would like a reply.Please contact us by email if you have any questions.