Regulatory Affairs Schedule

Live online Classroom		Jul	Sep	Oct	Nov	Dec	Jan
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
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK	Medical Devices			20
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects	Artificial Intelligence (AI) in Life Sciences				5
APIs in Focus: Understanding ICH, GMP and Supply Chain Excellence	GxP			21-22
An Essential Overview of Medical Information	Vigilance					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
An introduction to Risk Management ISO 14971:2019	Medical Devices			20
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
Best Practice for Writing Effective SOPs	0	14			26
Biological Evaluation of Medical Devices	Medical Devices	13-14
CAPA (Corrective and Preventative Action)	0					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 Application	0		30-1
Clinical Quality Management Systems	Clinical Research		17-18
Clinical Trial Regulatory Requirements	Clinical Research		14-15
Cyber Security for Medical Devices	Medical Devices			8-9
Digital CMC: The Key To Realising Pharma 4.0 New for 2026	0					4
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
Introduction to the In-Vitro Diagnostic Regulation (IVDR)	Medical Devices			15-16
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					8-9
Mastering CTD Submissions in the MENA Region	0				26
Mastering Computer System Validation	GxP					10-11
Medical Device Regulation in the Eurasian Union, Russia and the CIS	Medical Devices					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
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations	Medical Devices
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products Updated for 2026	Medical Devices		14-15
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					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
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					3
The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA	Animal Health
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
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR	Medical Devices		21
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				30
Variations to Marketing Authorisations	0				11-12
Veterinary Pharmaceutical Submissions in the EU	Animal Health				19-20