Manufacture of Investigational Medicinal Products – Frequently Asked Questions
Posted by:
Alan Moon, Posted on:
-
Categories:
Compliance matters, Good clinical practice, Good manufacturing practice
GMP and GCP Inspectors work closely with MHRA Clinical Trials and regularly provide support to help answer a wide range of stakeholder queries which relate to the manufacture, import, labelling, licencing requirements and general handling of Investigational Medicinal Products (IMPs). …
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