Introductory courses in regulatory affairs

Foundation courses logoIf you want to build a solid and comprehensive foundation in regulatory affairs, our Introductory Courses are for you. Choose from courses focusing on pharmaceutical or medical devices.

The courses are presented by speakers and facilitators from industry and agencies, all respected authorities in their fields.

Each four-day course (or three-day for the annual Medical Devices Introductory Course) covers all aspects of the product development process and provides a sound overview of EU legislation and regulatory procedures. We look at the central role regulatory affairs plays in modern healthcare companies and the development cycle of new drugs and devices.

Spring Intro Course (Pharmaceuticals) banner

Upcoming courses

Begin DateTitleDescriptionCityCountry
31/03/2020The Spring Introductory Course (Pharmaceuticals)An Introduction to Pharmaceutical Regulatory Affairs (Module 0 of the MSc Regulatory Affairs). This course covers all aspects of the product development process, and provides a sound overview of EU legislation and regulatory procedures, including the central role regulatory affairs plays in modern healthcare companies.CheshuntUnited KingdomIC12020
08/07/2020The Medical Device Introductory Course(Module 13 of the MSc Medical Devices) Providing those new to Medical Device Regulatory Affairs with an understanding of the regulatory requirements for medical devices in the EU.Kings LangleyUnited KingdomINTROMD20
17/11/2020The Autumn Introductory Course (Pharmaceuticals)An Introduction to Pharmaceutical Regulatory Affairs (Module 0 of the MSc Regulatory Affairs). This course covers all aspects of the product development process, and provides a sound overview of EU legislation and regulatory procedures, including the central role regulatory affairs plays in modern healthcare companies.BerlinGermanyIC22020

 


Why should I attend?

Why attend photo

The TOPRA Introductory Courses are recognised as the most comprehensive of their kind. The content for each course is up to date and researched by practising regulatory professionals.

These intensive courses provide a unique opportunity to exchange knowledge and experiences with your peers and build a personal network. You will also have access to international experts from industry and regulatory authorities.

You can expect to gain in confidence as a regulatory professional. The course proves your commitment to regulatory affairs and demonstrates that you have the foundation knowledge to progress your career.

This course has been supplied to UK delegates seeking employment via Job Centre Plus, part of the Department for Work and Pensions.


What will I learn?

The courses look at the big picture, covering not only EU legislation and regulatory procedures but also the central role regulatory affairs plays from design and development through to marketing authorisation and post-approval maintenance.


How will I learn?

Lectures are given by experts from the regulatory industry, contract houses and EU regulatory agencies. The formal presentations are combined with interactive workshops and breakout sessions.

At the end of each day we turn theory into practice by looking at a tailored case study, tackling realistic regulatory challenges. You will work in a team and develop your communication skills.

With a high facilitator-to-delegate ratio, there is always someone available to answer questions.


What previous attendees have said about our Intro courses:

Quotes photo"This course has given me a good foundation knowledge in a wide range of regulatory affairs activities, which I hope to build upon during my career."

"After being a consultant for 10 months and having heard of many of the topics, I now finally got a theoretical background. This greatly strengthened my position and confidence when working with various clients."

"The main learning points for me were a better understanding of the legal framework for obtaining MA in the EU. I have already been able to use this during client meetings in being able to provide better advice regarding the clinical development strategy."

"I have the wonderful notes to refer back to, which I will probably keep for the rest of my working career as my other colleagues have."