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Dr Gary Rees

Consultant
BPharm, PhD, CChem, MRSC, FCQI, CQP

A pharmacist with a Ph.D in Medicinal Chemistry, Gary has over 35 years diverse experience in the pharmaceutical industry, from pharmaceutical development to purchasing. Most of his time, however, has been spent in manufacturing, quality control and quality assurance, culminating in the role of Vice President, Quality & Compliance in Wyeth’s European, Mid-East and African region.

Gary’s experience stretches across the quality systems of a wide range of dosage forms and technologies, and he particularly enjoys the challenges of sterile manufacture.

He was formerly chairman of the British Pharmacopoeia Antibiotics Committee (Committee E), Vice Chairman of Committee A, and sat on the BP Commission for over 15 years.

He is also a former member of the European Federation of Pharmaceutical Industry Association’s (EFPIA) Anti-Counterfeiting Ad Hoc group, and is keenly aware of the risks of counterfeiting to the Industry and to patients globally.

Gary is eligible to act as a Qualified Person.

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NSF - DBA | Pharmaceutical, Medical Devices, Dietary Supplements, QP
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