Regulatory Affairs Schedule

Live online		Apr	May	Jun	Jul	Sep	Oct	Nov	Dec	Jan
Live online		2027								2028
A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products	Animal Health		6					2
A Practical Approach to Veterinary Vaccine Development and Registration in the EU	Animal Health					22-23
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects	Artificial Intelligence (AI) in Life Sciences		10					12
AI in Healthcare: Governance, Risk & Strategic Adoption New for 2027	Artificial Intelligence (AI) in Life Sciences					21
APIs in Focus: Understanding ICH, GMP and Supply Chain Excellence	GxP	28-29					20-21
An Essential Overview of Medical Information	Vigilance			21					2
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices	Medical Devices		13					8
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals	Medical Devices		7					18
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices	Medical Devices
An Overview of EU and UK Regulatory Affairs	0					20-21
Animal Feed and Feed Additive Registration in China and Thailand	Animal Health	15					21
Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions New for 2026	0			9					8
Biological Evaluation of Medical Devices	Medical Devices				1-2
CAPA (Corrective and Preventative Action)	0			14					3
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products	GxP	22-23					18-19
Cleanroom Requirements for Medical Device Manufacturers	Medical Devices					20
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Applications	0					29-30
Clinical Quality Management Systems (CQMS): A Practical Guide to Inspection Readiness	Clinical Research					16-17
Clinical Trial Regulatory Requirements	Clinical Research					23-24
EU Pharmaceutical Regulations and Strategy	0						4-5
EU Proposed Pharmaceutical Legislation Changes	0				7
FDA Approval Process for Medical Devices	Medical Devices		24-25					30-1
How the Pharmaceutical and Biotech Industries Work: From Molecule to Market	0					27
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3	Animal Health	12-13					14-15
Masterclass: Market Authorisation of AI-enabled Medical Devices	Artificial Intelligence (AI) in Life Sciences			28-29					7-8
Mastering CTD Submissions in the MENA Region	0		25					25
Mastering Computer System Validation	GxP			16-17					9-10
Medical Device Cybersecurity and Regulatory Compliance	Medical Devices					30-1
Medical Device Regulation in the Eurasian Union, Russia and the CIS	Medical Devices			29-30					7-8
Medical Device Regulations in Asia-Pacific Markets	Medical Devices					15-16
Medical Device Regulations in the Middle East and North Africa	Medical Devices		17-18					17-18
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations	Medical Devices			21-25
Navigating EU Product Classification: Foods, Supplements & Herbal Medicines Masterclass Updated for 2026	0			10					3
Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests New for 2026	Medical Devices
Non-Conformance and Corrective Action for Medical Device Manufacturers	Medical Devices
Orphan Drug Regulatory Masterclass: EU & US Insights	0					28
Pharmaceutical Regulatory Affairs in Asia	0						19-21
Pharmaceutical Regulatory Affairs in China	0		19-20					24-25
Pharmaceutical Regulatory Affairs in Russia, Eurasian Union and the CIS	0					29-30
Pharmaceutical Regulatory Affairs in the Middle East	0	12-13					19-20
Pharmaceutical Regulatory Affairs in the Middle East and North Africa New for 2026	0			7-9
Registration of Veterinary Pharmaceuticals in China New for 2026	Animal Health	15					21
Regulatory Compliance and Safety Standards for Aesthetic Devices New for 2026	Cosmetics
Sterilization of Medical Devices	Medical Devices	22-23					11-12
The 2024 EU AI Act New for 2026	Artificial Intelligence (AI) in Life Sciences			22					2
The Common Technical Document	GxP	13-14					20-21
The FDA Drug Approval Process	0					23-24
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry	0	19-20					11-12
UK Conformity Assessed (UKCA) Marking for Medical Devices	Medical Devices	14					20
US FDA - Understanding Key Factors When Working with the FDA	Biopharma				7
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers	Medical Devices			7				29
Variations to Marketing Authorisations	0			14-15				10-11
Veterinary Pharmaceutical Submissions in the EU	Animal Health		17-18					18-19
Writing Inspection-Ready SOPs: Best Practice for Compliance and Control	0		6					25