Consultant, Pharma Biotech

Email: pharmamail@nsf.org
Phone: +44(0)1751 432999
Country: United Kingdom

Richard Funnell has 30 years’ experience in the pharmaceutical industry in both regulatory and industrial roles. He worked within the MHRA GMP inspectorate from 2003 until 2014, including seven years as a senior inspector when he was the lead for investigational medicinal products (IMP) Good Manufacturing Practices (GMPs).

While at the MHRA, he inspected over 300 different sites within the UK and overseas. He also presented at numerous conferences and symposia on a wide variety of GMP-related topics.

Before joining the MHRA, Mr. Funnell  spent 17 years in industry in a number of roles in the production and quality assurance of tablets, oral liquids and sterile products.

He became QP eligible in 2002 after attending the NSF series of courses.

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