Regulatory Affairs Training Course Calendar

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Our Regulatory Affairs calendar for the next 12 months:

Live online Classroom 2025 2026
Dec Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov
A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products Regulatory Affairs 7 3
A Practical Approach to Veterinary Vaccine Development and Registration in the EU Regulatory Affairs 10-11 23-24
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Regulatory Affairs 29 20
Advanced Regulatory Affairs for Medical Devices Regulatory Affairs
An Essential Overview of Medical Information Regulatory Affairs 4 22
An Essential Overview of the Pharmaceutical and Biotech Industries Regulatory Affairs 12 28
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices Regulatory Affairs
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 8 19
An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices Regulatory Affairs
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Regulatory Affairs 21 18
An Introduction to the Medical Device Regulation Regulatory Affairs
An introduction to Risk Management ISO 14971:2019 Regulatory Affairs 27 20
Animal Feed and Feed Additive Registration in China and Thailand Regulatory Affairs
Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions Regulatory Affairs 10 10
Best Practice for Writing Effective SOPs Regulatory Affairs 4 26 14 26
Biological Evaluation of Medical Devices Regulatory Affairs
CAPA (Corrective and Preventative Action) Regulatory Affairs 5 15
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products Regulatory Affairs 23-24 19-20
Classification of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs
Cleanroom Requirements for Medical Device Manufacturers Regulatory Affairs 23 21
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Regulatory Affairs 16-17 30-1
Cyber Security for Medical Devices Regulatory Affairs 19-20 28-29
Data Innovation for AI-enabled Medical Devices Regulatory Affairs
Developing and Managing Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs
EU Pharmaceutical Regulations & Strategy Regulatory Affairs 2-3 5-6
EU Proposed Pharmaceutical Legislation Changes Regulatory Affairs 19 1
FDA Approval Process for Medical Devices Regulatory Affairs 2-3 30-1
Global Market Access for Medical Device Software Regulatory Affairs 1-2 8-9 30-1
Human Factors and Usability Engineering in the Development of Drug Delivery Products Regulatory Affairs 11-12 15-16
ICH Q9(R1) Quality Risk Management (QRM) Regulatory Affairs
Innovate: The MedTech Series – The 2024 EU AI Act Regulatory Affairs
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 16-17 15-16
Market Authorisation of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs
Masterclass: Market Authorisation of AI-enabled Medical Devices Regulatory Affairs 19-20 17-18
Medical Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 9-10 30-1
Medical Device Regulations in Asia-Pacific Markets Regulatory Affairs 3-4 16-17
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 18-19 18-19
Medical Device Single Audit Programme (MDSAP) Regulatory Affairs 25-26 25-26
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products Regulatory Affairs 2-3 14-15
Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests Regulatory Affairs 15 9
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 11
Orphan Drug Regulatory Masterclass: EU & US Insights Regulatory Affairs 4 6
Pharmaceutical Regulatory Affairs in Africa Regulatory Affairs 6-7 3-4
Pharmaceutical Regulatory Affairs in Asia Regulatory Affairs 24-26 7-9
Pharmaceutical Regulatory Affairs in China Regulatory Affairs 12-13 25-26
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union Regulatory Affairs 5-6 30-1
Pharmaceutical Regulatory Affairs in the Middle East Regulatory Affairs 24-25 20-21
Pharmaceutical Regulatory Affairs in the Middle East and North Africa Regulatory Affairs
Registration of Veterinary Pharmaceuticals in China Regulatory Affairs
Regulatory Affairs for Support Staff Regulatory Affairs 11-12 21-22
Regulatory Compliance and Safety Standards for Aesthetic Devices Regulatory Affairs 5 12
Sterilization of Medical Devices Regulatory Affairs
The Common Technical Document (CTD) Submission in the MENA Region Regulatory Affairs 19 27
The FDA Drug Approval Process Regulatory Affairs 23-24 24-25
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry Regulatory Affairs 27-28 12-13
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Regulatory Affairs 4 21
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 15 21
US FDA - Understanding Key Factors When Working with the FDA Regulatory Affairs 12 25
Understanding Active Pharmaceutical Ingredients (APIs) Regulatory Affairs 29-30 21-22
Understanding Computer System Validation (CSV) Regulatory Affairs 17-18
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs
Variations to Marketing Authorisations Regulatory Affairs 2-3 11-12
Veterinary Pharmaceutical Submissions in the EU Regulatory Affairs 18-19 19-20