
Presented by
Management Forum
Drive regulatory success with this two-day course for RA and Regulatory Operations professionals. Master practical project management tools, stakeholder strategies, and risk planning through a focused, real-world regulatory case study.
20-21 April 2026
+ 8-9 October 2026 »
from £999
Regulatory Affairs (RA) plays a pivotal role in ensuring that medicines reach patients efficiently and compliantly. With increasing global complexity - multiple markets, evolving health authority requirements, accelerated pathways, and cross-functional dependencies - effective project management has become essential for RA professionals at every level.
This two-day interactive course is designed specifically for Regulatory Affairs and Regulatory Operations professionals who plan, co-ordinate, and deliver successful submissions and lifecycle projects. Through a blend of technical project management tools and interpersonal leadership skills, participants will learn how to manage timelines, stakeholders, and regulatory deliverables with confidence and precision.
Participants will also gain practical insights into risk management, resource allocation, and communication strategies tailored to the regulatory environment. The programme includes interactive sessions applying techniques to a regulatory case study, with the option to use your own project for real-world relevance. There is no need to disclose any confidential information.
This training course is part of our collection of Leadership & Management Training Courses which focus on leadership, innovation, strategy, communication, finance, problem solving and conflict management, to name a few key areas.
By the end of the course, participants will be able to:
This course is designed for professionals working in Regulatory Affairs and Regulatory Operations across pharmaceuticals, biotechnology, and medical devices, including:
It is ideal for both newer professionals seeking structure in managing regulatory projects and experienced managers aiming to enhance cross-functional efficiency and leadership impact.
Dr Laura Brown is an independent pharmaceutical project management and training consultant and Senior Lecturer for the MSc in Clinical Research at the School of Pharmacy, University of Cardiff. Laura has more than 25 years’ experience of managing projects in the pharmaceutical industry and has worked for several companies including Wellcome, Hoechst Marion Roussel, Good Clinical Research Practices and Phoenix International. Laura has completed an MBA, with specialisation in project management. She is also the external project management expert for a pharmaceutical e-learning MSc module in project management and the author of two books on the subject including the leading title, Project Management for the Pharmaceutical Industry.
NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:
Please contact us for pricing if you are interested in booking 5 or more delegates
20-21 April 2026
Live online
09:30-17:00 UK (London) (UTC+01)
10:30-18:00 Paris (UTC+02)
04:30-12:00 New York (UTC-04)
Course code 16836
Until 16 Mar
Not ready to book yet?
for 7 days, no obligation
8-9 October 2026
Live online
09:30-17:00 UK (London) (UTC+01)
10:30-18:00 Paris (UTC+02)
04:30-12:00 New York (UTC-04)
Course code 16838
Until 03 Sep
Not ready to book yet?
for 7 days, no obligation
* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price; and apply only when booking multiple delegates on the same date.
Multiple colleagues? See above for details of our discounts for 2, 3, or 4 delegates. For more, talk to one of our training experts to discuss how to: