MR. PAUL K. MOORE, BSC, CBIOL, MRSB, CQP, MCQI
He has traveled extensively throughout the world working with many of the major multinationals working in both API and finished dose manufacturing facilities. This has included working with, for example: – US-based biological facilities on behalf of a major EU multinational, API, and finished dose producers in China, as well as Oral Solid Dose and Sterile facilities in the US, UK Mexico, and India where he lived for 3 years.
He has carried out inspections and worked in facilities on a worldwide basis and has extensive knowledge of global regulatory aspects, especially within Europe and UK.
He has been a Qualified Person under permanent provisions Euro Directive 75 / 319 for nearly 30 years.
He has performed many Quality Audits for international companies and acted as an advisor for corrective actions in many plants. Importantly throughout his career, he has had hands-on experience in API and formulation manufacturing and understands the business issues that make a successful pharmaceutical company.
He is a Chartered Biologist, a Chartered Quality Professional, and a Member of the European QP Association as well as a member of the Pharmaceutical & Healthcare Sciences Society and the Pharmaceutical Quality Group in the UK
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