Regulatory Affairs Training Course Calendar

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Our Regulatory Affairs calendar for the next 12 months:

Live online Classroom 2024 2025
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 5 1
A Practical Approach to Veterinary Vaccine Development and Registration in the EU Regulatory Affairs 13-14
A Regulatory Update on Animal Feed and Feed Additives in the EU, USA and China Regulatory Affairs 2-3
A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK Regulatory Affairs 30 21
Advanced Regulatory Affairs for Medical Devices Regulatory Affairs 13-14 3-4 2-3
An Essential Overview of Medical Information Regulatory Affairs 29 14 18
An Essential Overview of the Medical Device Industry Regulatory Affairs 14 3
An Essential Overview of the Pharmaceutical and Biotech Industries Regulatory Affairs 16 12 22
An Introduction to Ethylene Oxide (EO) Sterilization for Medical Devices Regulatory Affairs 11 1
An Introduction to Human Factors for Pharmaceutical and Medical Device Professionals Regulatory Affairs 17 9
An Introduction to ISO 11607 - Packaging for Terminally Sterilized Medical Devices Regulatory Affairs 22
An Introduction to ISO 13485: 2016 - Quality Management System (QMS) for Medical Devices Regulatory Affairs 13 3
An Introduction to the Medical Device Regulation Regulatory Affairs 25-27 16-18
An introduction to Risk Management ISO 14971:2019 Regulatory Affairs 11 11
Animal Feed and Feed Additive Registration in China and Thailand Regulatory Affairs 27 26 23
Antimicrobial Resistance (AMR) and 'One Health': Current Challenges, Regulatory Frontiers and Future Solutions Regulatory Affairs 9 17
Best Practice for Writing Effective SOPs Regulatory Affairs 12 27 17
Biological Evaluation of Medical Devices Regulatory Affairs 15-16 15-16 15-16
CAPA (Corrective and Preventative Action) Regulatory Affairs 13 28 18
Chemistry, Manufacture and Control (CMC) - Regulatory Requirements for Biological Drug Products Regulatory Affairs 27-28 26-27 20-21
Classification of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 28 9
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application Regulatory Affairs 5-6 18-19 1-2
Cyber Security for Medical Devices Regulatory Affairs 28-29 8-9 11-12
Data Innovation for AI-enabled Medical Devices Regulatory Affairs 28 9
Deep Dive into the IVDR Annex XIII Regulatory Affairs 5 10
Developing and Managing Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 3 10
EU Pharmaceutical Regulations & Strategy Regulatory Affairs 10-11 9-10 6-7
EU Proposed Pharmaceutical Legislation Changes Regulatory Affairs 20 19 16
FDA Approval Process for Medical Devices Regulatory Affairs 2-3 31-1 22-23
Global Pharmaceutical Regulatory Affairs Summer School Regulatory Affairs 9-13
Human Factors and Usability Engineering in the Development of Drug Delivery Products Regulatory Affairs 5-6 15-16 13-14 16-17
ICH Q9(R1) Quality Risk Management (QRM) Regulatory Affairs 29 12 9
Introduction to the In-Vitro Diagnostic Regulation (IVDR) Regulatory Affairs 5-6 16-17
Introduction to the New Performance Evaluation Requirements Mandated Under the IVDR (2017/746) Regulatory Affairs 4 9
Managing Competence within the Medical Device Industry Regulatory Affairs 26 11
Market Authorisation of Software as a Medical Device (SaMD) and Medical Device Software (MDSW) Regulatory Affairs 26-27 7-8
Masterclass: Market Authorisation of AI-enabled Medical Devices Regulatory Affairs 4 11
Medical Device Regulation in the Eurasian Union, Russia and the CIS Regulatory Affairs 9-10 3-4 23-24
Medical Device Regulations in the Middle East and North Africa Regulatory Affairs 10-11 23-24
Medical Device Single Audit Programme (MDSAP) Regulatory Affairs 28-29 24-25 10-11
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations Regulatory Affairs 18-21
Navigating China’s API Regulations: An Essential Guide to DMF Registration Regulatory Affairs 12 23 23
Navigating EU and FDA Regulations for Drug/Device and Device/Drug Combination Products Regulatory Affairs 21-22 19-20 10-11
Navigating Regulatory Compliance Whilst Developing and Distributing PCR-Based IVD Tests Regulatory Affairs 6 26
Non-Conformance and Corrective Action for Medical Device Manufacturers Regulatory Affairs 12 10 18
Pharmaceutical Regulatory Affairs in Africa Regulatory Affairs 19-20 24-25 16-17 21-22
Pharmaceutical Regulatory Affairs in Asia Regulatory Affairs 25-27 11-13 8-10
Pharmaceutical Regulatory Affairs in China Regulatory Affairs 10-11 31-1 25-26
Pharmaceutical Regulatory Affairs in Latin America Regulatory Affairs 25 18 22
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union Regulatory Affairs 6-7 19-20 2-3
Pharmaceutical Regulatory Affairs in the Middle East Regulatory Affairs 9-10 25-26 23-24 21-22
Post-Market Surveillance - Practical Application for Medical Devices and IVDs Regulatory Affairs 12 5 9
Practical Implementation of a Human Factors Study Regulatory Affairs 4-5 1-2
Registration of Veterinary Pharmaceuticals in China Regulatory Affairs 27 26 23
Regulatory Affairs for Support Staff Regulatory Affairs 27-28 12-13 22-23
Regulatory Strategies for Orphan Drugs Regulatory Affairs 10 23 7
Risk Management for Pharma and Biopharma Professionals Regulatory Affairs 4 6 7
Sterilization of Medical Devices Regulatory Affairs 3-4 5-6 16-17
The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA Regulatory Affairs 16-19
The Common Technical Document (CTD) Submission in the MENA Region Regulatory Affairs 28 13 1
The FDA Drug Approval Process Regulatory Affairs 2-3 24-25 11-12 7-8
The Medical Device School - From Concept to CE Marking Regulatory Affairs 2-6 9-13
The Regulatory Requirements on Nitrosamines in the Pharmaceutical Industry Regulatory Affairs 13-14 12-13 13-14
The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR and IVDR Regulatory Affairs 23 22 22
UK Conformity Assessed (UKCA) Marking for Medical Devices Regulatory Affairs 10 26 21
US FDA - Understanding Key Factors When Working with the FDA Regulatory Affairs 27 13 11
Understanding Active Pharmaceutical Ingredients (APIs) Regulatory Affairs 25-26 16-17
Understanding Computer System Validation (CSV) Regulatory Affairs 18-19 9-10
Unique Device Identification (UDI) and Labelling for Medical Device Manufacturers Regulatory Affairs 5 24 8
Variations to Marketing Authorisations Regulatory Affairs 28-29 6-7 3-4 15-16
Veterinary Pharmaceutical Submissions in the EU Regulatory Affairs 26-27 19-20