Companies across the pharmaceutical and biotechnology industry are subject to global agency regulations and industry guidance that govern medicine development and manufacturing. In the UK the Medicines and Healthcare products Regulatory Agency and European Medicines Agency (EMA) regulations, Industry Code of Practice and NICE clinical guidelines are designed to protect the public health by assuring the safety, effectiveness, and security of medicines.

EMIG works closely with NICE and EMIG’s Regulatory, Safety and Quality Group actively engages with the MHRA to ensure an open and collaborative approach to protecting the nation’s health.

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