Regulatory Affairs Training Course Calendar

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Our Regulatory Affairs calendar for the next 12 months:

Live online Classroom 2026
Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec
A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products Animal Health 7 3
A Practical Approach to Veterinary Vaccine Development and Registration in the EU Animal Health 10-11 23-24
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Medical Devices 29 20
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects Artificial Intelligence (AI) in Life Sciences 11 5
APIs in Focus: Understanding ICH, GMP and Supply Chain Excellence GxP 29-30 21-22
An Essential Overview of Medical Information Vigilance 22 3
An Essential Overview of the Pharmaceutical and Biotech Industries 0 12 28
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices Medical Devices 14 9
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Medical Devices 8 19
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Medical Devices 21 19
An Overview of EU and UK Regulatory Affairs 0 11-12 21-22
An introduction to Risk Management ISO 14971:2019 Medical Devices 27 20
Animal Feed and Feed Additive Registration in China and Thailand Animal Health 16 22
Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions 0 10 9
Best Practice for Writing Effective SOPs 0 26 14 26
Biological Evaluation of Medical Devices Medical Devices 21-22 13-14
CAPA (Corrective and Preventative Action) 0 15 4
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products GxP 23-24 19-20
Cleanroom Requirements for Medical Device Manufacturers Medical Devices 23 21
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application 0 16-17 30-1
Clinical Quality Management Systems Clinical Research 23-24 17-18
Clinical Trial Regulatory Requirements Clinical Research 2-3 14-15
Cyber Security for Medical Devices Medical Devices 19-20 28-29
EU Pharmaceutical Regulations and Strategy 0 2-3 5-6
EU Proposed Pharmaceutical Legislation Changes 0 19 1
FDA Approval Process for Medical Devices Medical Devices 30-1 1-2
Global Market Access for Medical Device Software Medical Devices 8-9 30-1
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Medical Devices 16-17 15-16
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3 Animal Health 13-14 15-16
Masterclass: Market Authorisation of AI-enabled Medical Devices Artificial Intelligence (AI) in Life Sciences 29-30 8-9
Mastering CTD Submissions in the MENA Region 0 19 26
Mastering Computer System Validation GxP 17-18 10-11
Medical Device Regulation in the Eurasian Union, Russia and the CIS Medical Devices 30-1 8-9
Medical Device Regulations in Asia-Pacific Markets Medical Devices 3-4 16-17
Medical Device Regulations in the Middle East and North Africa Medical Devices 18-19 18-19
Medical Device Single Audit Programme (MDSAP) Medical Devices 25-26 25-26
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Medical Devices 26-30 22-26
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products Medical Devices 2-3 14-15
Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests Medical Devices 15 9
Non-Conformance and Corrective Action for Medical Device Manufacturers Medical Devices 19 10
Orphan Drug Regulatory Masterclass: EU & US Insights 0 4 6
Pharmaceutical Regulatory Affairs in Africa 0 6-7 3-4
Pharmaceutical Regulatory Affairs in Asia 0 24-26 20-22
Pharmaceutical Regulatory Affairs in China 0 3-4 25-26
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union 0 5-6 30-1
Pharmaceutical Regulatory Affairs in the Middle East 0 24-25 20-21
Pharmaceutical Regulatory Affairs in the Middle East and North Africa 0 2-4
Registration of Veterinary Pharmaceuticals in China Animal Health 16 22
Regulatory Compliance and Safety Standards for Aesthetic Devices Cosmetics 12 4
Sterilization of Medical Devices Medical Devices 23-24 15-16
The 2024 EU AI Act Artificial Intelligence (AI) in Life Sciences 23 3
The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA Animal Health 15-18
The Common Technical Document GxP 27-28 14-15 21-22
The FDA Drug Approval Process 0 23-24 24-25
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry 0 20-21 12-13
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Medical Devices 4 21
UK Conformity Assessed (UKCA) Marking for Medical Devices Medical Devices 15 21
US FDA - Understanding Key Factors When Working with the FDA Biopharma 12 25
Understanding Toxicology: A Guide for Non-Toxicologists 0 19 15
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Medical Devices 8 30
Variations to Marketing Authorisations 0 2-3 11-12
Veterinary Pharmaceutical Submissions in the EU Animal Health 18-19 19-20