Regulatory Control of Clinical Operations

The ‘Regulatory Control of Clinical Operations’ Masterclass will enable you to understand the practical and regulatory aspects of global clinical research. You will learn how to provide effective advice on the regulatory issues that are likely to arise during clinical programmes.

By attending this training course between 17 and 19 July 2024 (in-person in London, UK or online), you will also:

✅ Gain an insight into the complexities and requirements of pharmacovigilance in clinical research
✅ Understand the practical aspects of Good Clinical Practice (GCP) and how it supports clinical research
✅ Build a network that will support you for the rest of your career
✅ Earn 15 CPD hours

With an engaging programme, this course is the ideal next step for regulatory affairs professionals looking to develop their knowledge of clinical operations.

This course is part of our range of Masterclasses and is Module 5 in our MSc programme. Our Masterclasses are developed and delivered by a faculty of #expertspeakers and validated by the University of Hertfordshire.

Discounted rates are available for TOPRA MSc students, those working for regulatory or government agencies, academic institutions, charities, patient groups, or in full-time education.

TOPRA MSc students: £1,545 +VAT*
Delegates: £1,785 +VAT*

Discounted places:
A limited number of discounted places are available at the rates below. Please email us at [email protected] for a discount code before making your booking.

Those working for regulatory agencies, government agencies or academic institutions: £1,338.75 +VAT*
Those working for charities, patient groups or in full-time education: £892.50 +VAT*

*VAT, if applicable, is charged at the rate of 20%.