|
|
|
|
The world of veterinary regulatory affairs can be a confusing and complex place, particularly if you have no formal veterinary or regulatory affairs background. The purpose of this course is to provide you with a clear and concise understanding of the role played by regulatory affairs in obtaining and maintaining marketing authorisations for veterinary medicinal... Details
When: February 18, 2026
Where: London
|
This Masterclass will enable you to understand the practical and strategic regulatory issues relating to the development, maintenance and marketing of active devices. It will enable you to critically debate the commercial implications and the impaally debate the commercial implications and the impact of the regulations on product stakeholders.
When: December 2–4, 2025
Where: London
|
This Masterclass will enable you to understand the practical and strategic regulatory issues relating to the development, maintenance and marketing of active devices. It will enable you to critically debate the commercial implications and the impact of the regulations on product stakeholders. This Masterclass is also Module 20 of the MSc.
When: December 2–4, 2025
|
This course will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.
When: November 26, 2025
Where: London
|
This course will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.
When: November 26, 2025
Where: Online
|
This Masterclass will provide you with the theoretical background to data management, document management, electronic submissions, eCompliance regulatory information management and the new identification of Medicinal Products (IDMP) requirements, and find solutions to practical problems in this area. Deal with large volumes of data and deal with different data (from nonclinical to post-market pharmacovigilance). This Masterclass is also Module 12 of the... Details
When: November 18–20, 2025
|
This Masterclass will provide you with the theoretical background to data management, document management, electronic submissions, eCompliance regulatory information management and the new identification of Medicinal Products (IDMP) requirements, and find solutions to practical problems in this area. Deal with large volumes of data and deal with different data (from nonclinical to post-market pharmacovigilance). This Masterclass is Module 12 of the... Details
When: November 18–20, 2025
Where: London
|
This Masterclass is designed for regulatory affairs professionals to develop their understanding of the management and leadership skills needed to run a successful regulatory affairs department/organisation. The course is designed to be applicable to both drugs and device regulatory affairs by applying the principles taught to your own particular environment. This Masterclass is also Module 10 of the... Details
When: November 10–12, 2025
Where: London
|
This Masterclass is designed for regulatory affairs professionals to develop their understanding of the management and leadership skills needed to run a successful regulatory affairs department/organisation. The course is designed to be applicable to both drugs and device regulatory affairs by applying the principles taught to your own particular environment. This Masterclass is also Module 10 of the... Details
When: November 10–12, 2025
Where: Online
|
This course covers all aspects of the product development process, and provides a sound overview of EU and UK legislation and regulatory procedures, including the central role regulatory affairs plays in modern healthcare companies.
When: November 4–6, 2025
Where: London
|
This course covers all aspects of the product development process, and provides a sound overview of EU and UK legislation and regulatory procedures, including the central role regulatory affairs plays in modern healthcare companies.
When: November 4–6, 2025
|
There are regulatory processes and procedures to expedite approval and access, and to help support the development of medicines for the treatment of rare diseases. This course will provide key information about those regulatory processes and first-hand insights on how to get the best out of them.
When: October 30, 2025
Where: London
|
There are regulatory processes and procedures to expedite approval and access, and to help support the development of medicines for the treatment of rare diseases. This course will provide key information about those regulatory processes and first-hand insights on how to get the best out of them.
When: October 30, 2025
Where: Online
|
This course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.
When: October 28, 2025
Where: London
|
This course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.
When: October 28, 2025
Where: Online
|
This module primarily focusing on the In Vitro Diagnostic Regulation, this course will present the latest information covering the new regulation and how this differs from the In Vitro Diagnostic Directive in the EU and other jurisdictions. This Masterclass is also Module 19 of the MSc.
When: October 20–22, 2025
Where: London
|
This Masterclass primarily focusing on the In Vitro Diagnostic Regulation, this course will present the latest information covering the new regulation and how this differs from the In Vitro Diagnostic Directive in the EU and other jurisdictions. This Masterclass is also Module 19 of the MSc.
When: October 20–22, 2025
|
This two-day workshop will provide an overview with practical advice from regulators and industry on the process of designing and conducting clinical trials from phase I through phases II, III and even clinical trials considerations beyond drug marketing approval.
When: October 14–15, 2025
Where: London
|
This two-day workshop will provide an overview with practical advice from regulators and industry on the process of designing and conducting clinical trials from phase I through phases II, III and even clinical trials considerations beyond drug marketing approval.
When: October 14–15, 2025
Where: Online
|
The course will provide a comprehensive overview of the regulatory framework on Rx to OTC switch in Europe and the specificities of non-prescription medicines. It will also provide a number of examples and concrete cases to help understanding and turning theory into practice.
When: October 8, 2025
Where: Online
|
This Masterclass will provide you with an understanding of the regulatory landscape across South/East Asia. This Masterclass is also Module 25 of the MSc.
When: October 7–9, 2025
|
This Masterclass will provide you with an understanding of the regulatory landscape across South/East Asia. This Masterclass is also Module 25 of the MSc.
When: October 7–9, 2025
Where: London
|
Designed for start-ups, SMEs and Academia, our 2025 regulatory update is a one-day event which will take place on 1 October as part of the 2025 TOPRA Annual Symposium.
When: October 1, 2025
Where: Berlin
|