New HTAF GMP facility receives MHRA certification

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Clinical researchers can use the new, state-of-the-art GMP Facility at the Healthcare Technology Accelerator Facility (HTAF) to obtain high-quality medicinal products more quickly and efficiently. The GMP (Good Manufacturing Practice) Facility provides researchers and commercial partners with access to API manufacturing as well as a full range of sterile and non-sterile capabilities, from formulation, sterilisation and storage, to labelling, certification and distribution. Following a rigorous certification process, the Facility has obtained Medicines and Healthcare Products Regulatory Agency (MHRA) approval to import and manufacture Investigational Medicinal Products (IMPs) for use in human clinical trials.

Watch a video showcasing the capabilities and capacity of the Healthcare Technology Facility’s Sterile Fill unit here!)