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Drug licensing in veterinary euthanasia and assisted suicide in humans: a regulatory double standard

bmjspcare · 2025-11-09 · canonical JSON source

2 visible annotations · policy: published · automated confidence ≥ 75.00%

Document resource

In the United Kingdom (UK), the Medicines and Healthcare products Regulatory Agency (MHRA) 1 serves as the principal medicines regulatory authority, operating under the Human Medicines Regulations 2012.2 Its key role is to ensure that medicines are effective, safe and manufactured to consistently high standards.