Regulatory Affairs Training Course Calendar

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Our Regulatory Affairs calendar for the next 12 months:

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