Regulatory services in the UK for the pharmaceutical sector are managed by the Medicines and Healthcare products Regulatory Agency (MHRA). These services include drug licensing and approval, pharmacovigilance to monitor safety, and oversight of clinical trials. The MHRA also conducts inspections to ensure compliance with manufacturing and safety standards. Post-market surveillance ensures ongoing drug safety, while post-Brexit, the MHRA manages UK-specific regulatory requirements. Overall, these services ensure that medicines meet high standards of safety, efficacy, and quality.
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