Regulatory Affairs Schedule

Live online Classroom		Jun	Jul	Sep	Oct	Nov	Dec	Jan	Mar
Live online Classroom		2026						2027
A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products	Animal Health					3
A Practical Approach to Veterinary Vaccine Development and Registration in the EU	Animal Health			23-24
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects	Artificial Intelligence (AI) in Life Sciences					5
AI in Healthcare: Governance, Risk & Strategic Adoption New for 2026	Artificial Intelligence (AI) in Life Sciences			22					9
APIs in Focus: Understanding ICH, GMP and Supply Chain Excellence	GxP				21-22
An Essential Overview of Medical Information	Vigilance	22					3
An Essential Overview of the Pharmaceutical and Biotech Industries	0			28
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices	Medical Devices					9
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals	Medical Devices					19
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices	Medical Devices					19
An Overview of EU and UK Regulatory Affairs	0			21-22
Animal Feed and Feed Additive Registration in China and Thailand	Animal Health				22
Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions New for 2026	0						9
Biological Evaluation of Medical Devices	Medical Devices		13-14
CAPA (Corrective and Preventative Action)	0	15					4
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products	GxP				19-20
Cleanroom Requirements for Medical Device Manufacturers New for 2026	Medical Devices			21
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Applications	0			30-1
Clinical Quality Management Systems (CQMS): A Practical Guide to Inspection Readiness	Clinical Research			17-18
Clinical Trial Regulatory Requirements	Clinical Research			14-15
Cyber Security for Medical Devices	Medical Devices				8-9
EU Pharmaceutical Regulations and Strategy	0				5-6
EU Proposed Pharmaceutical Legislation Changes	0		1
FDA Approval Process for Medical Devices	Medical Devices						1-2
Global Market Access for Medical Device Software New for 2026	Medical Devices					30-1
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3	Animal Health				15-16
Masterclass: Market Authorisation of AI-enabled Medical Devices	Artificial Intelligence (AI) in Life Sciences	29-30					8-9
Mastering CTD Submissions in the MENA Region	0					26
Mastering Computer System Validation	GxP	17-18					10-11
Medical Device Regulation in the Eurasian Union, Russia and the CIS	Medical Devices	30-1					8-9
Medical Device Regulations in Asia-Pacific Markets	Medical Devices			16-17
Medical Device Regulations in the Middle East and North Africa	Medical Devices					18-19
Medical Device Single Audit Programme (MDSAP)	Medical Devices	25-26				25-26
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations	Medical Devices	22-26
Navigating EU Product Classification: Foods, Supplements & Herbal Medicines Masterclass Updated for 2026	0	11					4
Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests New for 2026	Medical Devices					9
Non-Conformance and Corrective Action for Medical Device Manufacturers	Medical Devices	19					10
Orphan Drug Regulatory Masterclass: EU & US Insights	0				6
Pharmaceutical Regulatory Affairs in Africa	0					3-4
Pharmaceutical Regulatory Affairs in Asia	0				20-22
Pharmaceutical Regulatory Affairs in China	0					25-26
Pharmaceutical Regulatory Affairs in Russia, Eurasian Union and the CIS	0			30-1
Pharmaceutical Regulatory Affairs in the Middle East	0				20-21
Pharmaceutical Regulatory Affairs in the Middle East and North Africa New for 2026	0	2-4
Registration of Veterinary Pharmaceuticals in China New for 2026	Animal Health				22
Regulatory Compliance and Safety Standards for Aesthetic Devices New for 2026	Cosmetics						4
Sterilization of Medical Devices	Medical Devices				12-13
The 2024 EU AI Act New for 2026	Artificial Intelligence (AI) in Life Sciences	23					3
The Common Technical Document	GxP				21-22
The FDA Drug Approval Process	0			24-25
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry	0				12-13
UK Conformity Assessed (UKCA) Marking for Medical Devices	Medical Devices				21
US FDA - Understanding Key Factors When Working with the FDA	Biopharma					25
Understanding Toxicology: A Guide for Non-Toxicologists New for 2026	0		15
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers	Medical Devices	8				30
Variations to Marketing Authorisations	0					11-12
Veterinary Pharmaceutical Submissions in the EU	Animal Health					19-20
Writing Inspection-Ready SOPs: Best Practice for Compliance and Control	0		14			26