Regulatory Affairs Training Course Calendar

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Our Regulatory Affairs calendar for the next 12 months:

Live online Classroom 2026 2027
Jul Aug Sep Oct Nov Dec Jan Feb Mar Apr May Jun
A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products Animal Health 3
A Practical Approach to Veterinary Vaccine Development and Registration in the EU Animal Health 23-24
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Medical Devices 20
AI & ML in Clinical Trials: Fundamentals, Applications, and Regulatory Aspects Artificial Intelligence (AI) in Life Sciences 5
APIs in Focus: Understanding ICH, GMP and Supply Chain Excellence GxP 21-22
An Essential Overview of Medical Information Vigilance 3
An Essential Overview of the Pharmaceutical and Biotech Industries 0 28
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices Medical Devices 9
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Medical Devices 19
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Medical Devices 19
An Overview of EU and UK Regulatory Affairs 0 21-22
An introduction to Risk Management ISO 14971:2019 Medical Devices 20
Animal Feed and Feed Additive Registration in China and Thailand Animal Health 22
Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions 0 9
Best Practice for Writing Effective SOPs 0 14 26
Biological Evaluation of Medical Devices Medical Devices 13-14
CAPA (Corrective and Preventative Action) 0 4
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products GxP 19-20
Cleanroom Requirements for Medical Device Manufacturers Medical Devices 21
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application 0 30-1
Clinical Quality Management Systems Clinical Research 17-18
Clinical Trial Regulatory Requirements Clinical Research 14-15
Cyber Security for Medical Devices Medical Devices 8-9
EU Pharmaceutical Regulations and Strategy 0 5-6
EU Proposed Pharmaceutical Legislation Changes 0 1
FDA Approval Process for Medical Devices Medical Devices 1-2
Global Market Access for Medical Device Software Medical Devices 30-1
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Medical Devices 15-16
Managing Service Providers including CRO and CMOs oversight to comply with ICH GCP R3 Animal Health 15-16
Masterclass: Market Authorisation of AI-enabled Medical Devices Artificial Intelligence (AI) in Life Sciences 8-9
Mastering CTD Submissions in the MENA Region 0 26
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 16-17
Medical Device Regulations in the Middle East and North Africa Medical Devices 18-19
Medical Device Single Audit Programme (MDSAP) Medical Devices 25-26
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Medical Devices
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products Medical Devices 14-15
Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests Medical Devices 9
Non-Conformance and Corrective Action for Medical Device Manufacturers Medical Devices 10
Orphan Drug Regulatory Masterclass: EU & US Insights 0 6
Pharmaceutical Regulatory Affairs in Africa 0 3-4
Pharmaceutical Regulatory Affairs in Asia 0 20-22
Pharmaceutical Regulatory Affairs in China 0 25-26
Pharmaceutical Regulatory Affairs in Russia, Eurasian Union and the CIS 0 30-1
Pharmaceutical Regulatory Affairs in the Middle East 0 20-21
Pharmaceutical Regulatory Affairs in the Middle East and North Africa 0
Registration of Veterinary Pharmaceuticals in China Animal Health 22
Regulatory Compliance and Safety Standards for Aesthetic Devices Cosmetics 4
Sterilization of Medical Devices Medical Devices 12-13
The 2024 EU AI Act Artificial Intelligence (AI) in Life Sciences 3
The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA Animal Health
The Common Technical Document GxP 21-22
The FDA Drug Approval Process 0 24-25
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry 0 12-13
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Medical Devices 21
UK Conformity Assessed (UKCA) Marking for Medical Devices Medical Devices 21
US FDA - Understanding Key Factors When Working with the FDA Biopharma 25
Understanding Toxicology: A Guide for Non-Toxicologists 0 15
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Medical Devices 30
Variations to Marketing Authorisations 0 11-12
Veterinary Pharmaceutical Submissions in the EU Animal Health 19-20