Home » MHRA Seeks Input on Plan to Streamline AE Reporting
MHRA Seeks Input on Plan to Streamline AE Reporting
The UK’s Medicines and Healthcare products Regulatory Agency is considering streamlining its collection of adverse event and incident reports by consolidating five reporting systems into one. Looking to increase overall incident reports, the agency would combine the systems under the most well-organized one, the Yellow Card Scheme, which currently is used to report side effects or adverse reactions to drugs.
International Medical Device Regulatory Monitor
International Medical Device Regulatory Monitor
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