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The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry (October 12-13, 2026)

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AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects (November 5, 2026)

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Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions (December 9, 2026)

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An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices (November 19, 2026)

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UK Conformity Assessed (UKCA) Marking for Medical Devices (October 21, 2026)

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A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK (October 20, 2026)

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How to Perform Bullet-Proof Good Distribution Practices (GDP) and Good Storage Practices (GSP) Audits (December 10-11, 2026)

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Digital CMC: The Key To Realising Pharma 4.0 (December 4, 2026)

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The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR (September 21, 2026)

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US FDA - Understanding Key Factors When Working with the FDA (November 25, 2026)

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