Regulatory Affairs Schedule

Live online Classroom		Dec	Jan	Mar
Live online Classroom		2026	2027
A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products	Animal Health
A Practical Approach to Veterinary Vaccine Development and Registration in the EU	Animal Health
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects	Artificial Intelligence (AI) in Life Sciences
AI in Healthcare: Governance, Risk & Strategic Adoption New for 2026	Artificial Intelligence (AI) in Life Sciences			9
APIs in Focus: Understanding ICH, GMP and Supply Chain Excellence	GxP
An Essential Overview of Medical Information	Vigilance	3
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices	Medical Devices
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals	Medical Devices
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices	Medical Devices
An Overview of EU and UK Regulatory Affairs	0
Animal Feed and Feed Additive Registration in China and Thailand	Animal Health
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
CAPA (Corrective and Preventative Action)	0	4
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products	GxP
Cleanroom Requirements for Medical Device Manufacturers New for 2026	Medical Devices
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Applications	0
Clinical Quality Management Systems (CQMS): A Practical Guide to Inspection Readiness	Clinical Research
Clinical Trial Regulatory Requirements	Clinical Research
Cyber Security for Medical Devices	Medical Devices
EU Pharmaceutical Regulations and Strategy	0
EU Proposed Pharmaceutical Legislation Changes	0
FDA Approval Process for Medical Devices	Medical Devices	1-2
Global Market Access for Medical Device Software New for 2026	Medical Devices
How the Pharmaceutical and Biotech Industries Work: From Molecule to Market	0
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3	Animal Health
Masterclass: Market Authorisation of AI-enabled Medical Devices	Artificial Intelligence (AI) in Life Sciences	8-9
Mastering CTD Submissions in the MENA Region	0
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
Medical Device Regulations in the Middle East and North Africa	Medical Devices
Medical Device Single Audit Programme (MDSAP)	Medical Devices
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations	Medical Devices
Navigating EU Product Classification: Foods, Supplements & Herbal Medicines Masterclass Updated for 2026	0	4
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	10
Orphan Drug Regulatory Masterclass: EU & US Insights	0
Pharmaceutical Regulatory Affairs in Africa	0
Pharmaceutical Regulatory Affairs in Asia	0
Pharmaceutical Regulatory Affairs in China	0
Pharmaceutical Regulatory Affairs in Russia, Eurasian Union and the CIS	0
Pharmaceutical Regulatory Affairs in the Middle East	0
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
Regulatory Compliance and Safety Standards for Aesthetic Devices New for 2026	Cosmetics	4
Sterilization of Medical Devices	Medical Devices
The 2024 EU AI Act New for 2026	Artificial Intelligence (AI) in Life Sciences	3
The Common Technical Document	GxP
The FDA Drug Approval Process	0
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry	0
UK Conformity Assessed (UKCA) Marking for Medical Devices	Medical Devices
US FDA - Understanding Key Factors When Working with the FDA	Biopharma
Understanding Toxicology: A Guide for Non-Toxicologists New for 2026	0
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers	Medical Devices
Variations to Marketing Authorisations	0
Veterinary Pharmaceutical Submissions in the EU	Animal Health
Writing Inspection-Ready SOPs: Best Practice for Compliance and Control	0