Regulatory Affairs Training Course Calendar

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Our Regulatory Affairs calendar for the next 12 months:

Live online Classroom 2025 2026
Nov Dec Jan Feb Mar Apr May Jun Jul Aug Sep Oct
A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products Regulatory Affairs 4 7
A Practical Approach to Veterinary Vaccine Development and Registration in the EU Regulatory Affairs 6-7 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
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects Regulatory Affairs 6 6
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 14
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 20 8
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Regulatory Affairs 21
An Overview of EU and UK Regulatory Affairs Regulatory Affairs 11-12 21-22
An introduction to Risk Management ISO 14971:2019 Regulatory Affairs 27 20
Animal Feed and Feed Additive Registration in China and Thailand Regulatory Affairs 16 22
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
Biological Evaluation of Medical Devices Regulatory Affairs 21-22 13-14
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
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
Clinical Quality Management Systems Regulatory Affairs 23-24 17-18
Clinical Trial Regulatory Requirements Regulatory Affairs 2-3 14-15
Cyber Security for Medical Devices Regulatory Affairs 19-20 28-29
EU Pharmaceutical Regulations and 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 8-9
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 16-17 15-16
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3 Regulatory Affairs 13-14 15-16
Masterclass: Market Authorisation of AI-enabled Medical Devices Regulatory Affairs 18-19 29-30
Mastering CTD Submissions in the MENA Region Regulatory Affairs 28 19
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 3-4 16-17
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 19-20 18-19
Medical Device Single Audit Programme (MDSAP) Regulatory Affairs 25-26
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Regulatory Affairs 26-30 22-26
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
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 11 19
Orphan Drug Regulatory Masterclass: EU & US Insights Regulatory Affairs 4 6
Pharmaceutical Regulatory Affairs in Africa Regulatory Affairs 6-7
Pharmaceutical Regulatory Affairs in Asia Regulatory Affairs 24-26 20-22
Pharmaceutical Regulatory Affairs in China Regulatory Affairs 26-27 3-4
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
Registration of Veterinary Pharmaceuticals in China Regulatory Affairs 16 22
Regulatory Compliance and Safety Standards for Aesthetic Devices Regulatory Affairs 5 12
Sterilization of Medical Devices Regulatory Affairs 23-24 15-16
The 2024 EU AI Act Regulatory Affairs 23
The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA Regulatory Affairs 15-18
The Common Technical Document Regulatory Affairs 24-25 27-28 14-15 21-22
The FDA Drug Approval Process Regulatory Affairs 23-24 24-25
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry Regulatory Affairs 20-21 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 26 12
Understanding Active Pharmaceutical Ingredients (APIs) Regulatory Affairs 29-30 21-22
Understanding Computer System Validation (CSV) Regulatory Affairs 24-25 17-18
Understanding Toxicology: A Guide for Non-Toxicologists Regulatory Affairs 19 15
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 8
Variations to Marketing Authorisations Regulatory Affairs 2-3
Veterinary Pharmaceutical Submissions in the EU Regulatory Affairs 25-26 18-19