The conference will open with a keynote presentation delivered by Ian Rees, Expert GMP Inspector, MHRA, on
Compliance Trends within the Pharmaceutical Industry: A Regulatory Perspective. A unique question
and answer opportunity will be available immediately following the keynote address.
Education will continue, as delegates and regulators participate throughout the two days in one of three comprehensive tracks: Biotech, Oral Solid Dosage / Containment and Process Validation, where they will discuss real industry issues on how to combine the best in science and engineering to deliver high-quality products and low-cost operations.
Through interactive sessions and workshops, delegates will learn methods to improve process efficiency and successful approaches to drive effective facility utilisation. Engage with speakers, fellow participants, and regulators, throughout the two days, and gain perspective on how to avoid costly compliance issues.
The programme will include speeches delivered by international industry and regulatory experts. Delegates will also have a unique opportunity to exchange views with the Irish Medicines Board.
These sessions are designed to help companies combine the best in science and engineering so they can deliver high-quality products with low-cost operations. You can be sure of this: you will return to your site with knowledge that will help your company address these real challenges.
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view the Agendas
High-Level Regulatory Speakers will Include:
Ian Rees, Expert GMP Inspector, MHRA, United Kingdom
Catherine McHugh, Executive Pharmaceutical Assessor, Irish Medicines Board, Ireland
Keith Pugh, Licensing Division Expert Assessor, MHRA, United Kingdom