Regulatory Affairs Training Course Calendar

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Our Regulatory Affairs calendar for the next 12 months:

Live online Live online Classroom 2024 2025
Apr May Jun Jul Aug Sep Oct Nov Dec Jan Mar Mar
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 4 5
A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products Regulatory Affairs 5
A Practical Approach to Veterinary Vaccine Development and Registration in the EU Regulatory Affairs 8-9 11-12
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Regulatory Affairs 22
Advanced Regulatory Affairs for Medical Devices Regulatory Affairs 4-7 7-8
An Essential Overview of Medical Information Regulatory Affairs 11 29
An Essential Overview of the Medical Device Industry Regulatory Affairs 8-9 8
An Essential Overview of the Pharmaceutical and Biotech Industries Regulatory Affairs 10 13
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices Regulatory Affairs 11
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 10 23
An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices Regulatory Affairs 21 18
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Regulatory Affairs 4 20
An Introduction to the Medical Device Regulation Regulatory Affairs 15-17 31-2 4-6
Animal Feed and Feed Additive Registration in China and Thailand Regulatory Affairs 21 16
Best Practice for Writing Effective SOPs Regulatory Affairs 18 12
Best Practices for Supplier Qualification in Life Science Regulatory Affairs 15-16 27-28 27-28 27-28
Biological Evaluation of Medical Devices Regulatory Affairs 16-17
CAPA (Corrective and Preventative Action) Regulatory Affairs 19 13
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products Regulatory Affairs 27-28 17-18
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Regulatory Affairs 19-20 2-3
Cyber Security for Medical Devices Regulatory Affairs 4-5 15-16
EU Pharmaceutical Regulations & Strategy Regulatory Affairs 10-11 14-15
EU Proposed Pharmaceutical Legislation Changes Regulatory Affairs 22 18
FDA Approval Process for Medical Devices Regulatory Affairs 19-20 10-11 2-3
Global Pharmaceutical Regulatory Affairs Summer School Regulatory Affairs 10-14
Human Factors and Usability Engineering in the Development of Drug Delivery Products Regulatory Affairs 5-6 17-20 5-6
ICH Q9(R1) Quality Risk Management (QRM) Regulatory Affairs 1 25
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 24-25 5-8
Managing Competence within the Medical Device Industry Regulatory Affairs 5
Medical Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 2-3 9-10
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 11-12 7-8
Medical Device Single Audit Programme (MDSAP) Regulatory Affairs 4-5 28-29
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Regulatory Affairs 22-25 9-12
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 19 12
Pharmaceutical Regulatory Affairs in Africa Regulatory Affairs 17-18 19-22
Pharmaceutical Regulatory Affairs in Asia Regulatory Affairs 12-14 9-11
Pharmaceutical Regulatory Affairs in China Regulatory Affairs 29-30 2-3 10-11
Pharmaceutical Regulatory Affairs in Latin America Regulatory Affairs 19 22
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union Regulatory Affairs 24-25 3-4
Pharmaceutical Regulatory Affairs in the Middle East Regulatory Affairs 26-27 9-10
Post-Market Surveillance - Practical Application for Medical Devices and IVDs Regulatory Affairs 6 10
Registration of Veterinary Pharmaceuticals in China Regulatory Affairs 21 16
Regulatory Affairs for Support Staff Regulatory Affairs 24-25
Regulatory Strategies for Orphan Drugs Regulatory Affairs 24 8
Risk Management for Pharma and Biopharma Professionals Regulatory Affairs 7 8
Sterilization of Medical Devices Regulatory Affairs 6-7 17-18
The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA Regulatory Affairs 17-20
The Common Technical Document (CTD) Submission in the MENA Region Regulatory Affairs 10 28
The FDA Drug Approval Process Regulatory Affairs 12-13 2-3
The Medical Device School - From Concept to CE Marking Regulatory Affairs 10-14 2-6
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Regulatory Affairs 24
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 15 19
US FDA - Understanding Key Factors When Working with the FDA Regulatory Affairs 12 27
Understanding Active Pharmaceutical Ingredients (APIs) Regulatory Affairs 17-18 18-19
Understanding Computer System Validation (CSV) Regulatory Affairs 24-25 25-26
Variations to Marketing Authorisations Regulatory Affairs 10-11 28-29
Veterinary Pharmaceutical Submissions in the EU Regulatory Affairs 11-12 26-27