Upcoming regulatory affairs courses & webinars

We offer a comprehensive programme of training courses and webinars on a wide range of regulatory affairs topics. Our courses and webinars are delivered by highly regarded experts from industry and government agencies and are suitable for professionals at all stages of their regulatory career.

Read more about the different regulatory affairs course categories and how these relate to your own career.

Our commitment to quality

TOPRA is proud to have provided gold standard training for regulatory affairs professionals for more than 40 years. Our commitment to the profession, to everyone who attends our training and to employers who entrust their staff development to us, is given in our Quality Statement.

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04/11/2025Overview of EU and UK Pharmaceutical Regulatory AffairsThis 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.LondonUnited KingdomIC0112025
04/11/2025Overview of EU and UK Pharmaceutical Regulatory AffairsThis 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. OnlineIC21125O
10/11/2025Leadership and Strategic Management in Regulatory AffairsThis 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 MSc.LondonUnited KingdomMSCM1025
10/11/2025Leadership and Strategic Management in Regulatory AffairsThis 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. OnlineMSCM1025O
19/11/2025Introduction To TOPRA - Make the Most of Your MembershipWelcome to TOPRA!  Make sure you join our webinar on 19 November 2025 to find out how you can make the most of your membership. OnlineMEMNOV25
20/11/2025Sponsored Webinar-Cell & Gene Therapies-key considerationsFREE SPONSORED WEBINAR - This session will focus on the obstacles faced when navigating regulations worldwide. It aims to evaluate market dynamics and emerging trends, how regulatory authorities are providing guidance, fostering collaborations, and establishing dedicated review pathways to facilitate development, and what changes to regulations can be expected in the European Union. As a bonus, we will also take a closer look at how to realize the immense potential of gene editing within the regulatory landscape. OnlineSPWBCLAR25
25/11/2025SponsoredWebinar-Product Information prep with QRD TemplatesFREE SPONSORED WEBINAR - This webinar will explore the QRD templates and provide practical guidance on how to use them while preparing product information.   . OnlineSWBILL2025
26/11/2025Essentials of European Medical Device Regulatory AffairsThis course will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.LondonUnited KingdomMDB1125
26/11/2025Essentials of European Medical Device Regulatory AffairsThis course will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment. OnlineMDB1125O
27/11/2025TOPRA Awards for Excellence 2025 - Finalist RegistrationCongratulations on being a Finalist! Join us at Plaisterers' Hall on 27 November 2025 at the Awards for Regulatory Excellence to celebrate the achievements of individuals, teams and organisations in the regulatory affairs community.LondonUnited KingdomAWARDNOM25
27/11/2025The Awards for Regulatory Excellence 2025Join us at Plaisterers' Hall, London on 27 November for the Awards for Regulatory Excellence to celebrate the achievements of individuals, teams and organisations in the regulatory affairs community.LondonUnited KingdomAWARDS2025
02/12/2025Regulation of Electrical, Electronic and Software DevicesThis 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.LondonUnited KingdomMDM202025
02/12/2025Regulation of Electrical, Electronic and Software DevicesThis 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. OnlineMSCM2025O
04/12/2025Sponsored Webinar-Joint Scientific ConsultationFREE SPONSORED WEBINAR - Covering the general requirements and eligibility for Joint Scientific Consultation, which topics are covered - from a regulatory and market access perspective; how to prepare from an operational (such as briefing book) and strategic (commercial and strategic implications) perspective OnlineSWCLINOV25
13/01/2026Data Management and Digitalisation in Regulatory AffairsGain the knowledge and practical skills to manage regulatory data in a digital world, from electronic submissions and eCompliance to regulatory information systems and IDMP implementation. This course is also Module 12 of the MSc programme. OnlineMSCM12225O
13/01/2026Data Management and Digitalisation in Regulatory AffairsGain the knowledge and practical skills to manage regulatory data in a digital world, from electronic submissions and eCompliance to regulatory information systems and IDMP implementation. This course is also Module 12 of the MSc programme.LondonUnited KingdomMSCM1225
27/01/2026Regulatory Environment in the Middle East and North AfricaMaster the complexities of the Middle East and North Africa's (MENA) evolving regulatory landscape and develop the insight to navigate regional challenges, drive compliance, and connect local developments to global strategies. This course is also Module 24 of the MSc programme.LondonUnited KingdomM240725F2F
27/01/2026Regulatory Environment in the Middle East and North AfricaMaster the complexities of the Middle East and North Africa's (MENA) evolving regulatory landscape and develop the insight to navigate regional challenges, drive compliance, and connect local developments to global strategies. This course is also Module 24 of the MSc programme. OnlineM24300725O
03/02/2026Managing People EffectivelyEffective leadership drives performance, engagement and retention. This course will help regulatory affairs professionals develop the skills and confidence to lead teams that are motivated, collaborative and deliver high-quality outcomes.LondonUnited KingdomCMPE25F
05/02/2026Essentials of European Pharmaceutical Regulatory AffairsThis course offers a basic but comprehensive understanding of European pharmaceutical regulatory affairs in a relaxed and interactive environment. Learn from industry experts and gain practical insights you can apply in your role.LondonUnited KingdomBAS0226F
05/02/2026Essentials of European Pharmaceutical Regulatory AffairsThis course offers a basic but comprehensive understanding of European pharmaceutical regulatory affairs in a relaxed and interactive environment. Learn from industry experts and gain practical insights you can apply in your role. OnlineBAS0226O
10/02/2026Regulatory Requirements for a New Active Substance: QualityGain the knowledge to interpret and advise on quality data requirements in pharmaceutical regulation, from manufacturing and validation to preparing CTD, IMPD and IND documentation. This Masterclass is also Module 3 of the MSc programme.FrankfurtGermanyMSCM32026F
10/02/2026Regulatory Requirements for a New Active Substance: QualityGain the knowledge to interpret and advise on quality data requirements in pharmaceutical regulation, from manufacturing and validation to preparing CTD, IMPD and IND documentation. This Masterclass is also Module 3 of the MSc programme. OnlineMSCM326O
17/02/2026Regulatory Document Writing and ManagementLearn to craft regulatory documents that are clear, accurate, and effective. This course blends theory and practice to equip you with the skills to manage submissions, communicate with regulators, and achieve optimal outcomes.LondonUnited KingdomDW26F
17/02/2026Regulatory Document Writing and ManagementLearn to craft regulatory documents that are clear, accurate, and effective. This course blends theory and practice to equip you with the skills to manage submissions, communicate with regulators, and achieve optimal outcomes. OnlineDW26O
24/02/2026The Regulatory Environment in South and East AsiaMaster the complexities of South and East Asia’s evolving regulatory landscape and develop strategies to support successful drug development across diverse markets. This Masterclass is also Module 25 of the MSc programme. OnlineM2525F2F
24/02/2026The Regulatory Environment in South and East AsiaMaster the complexities of South and East Asia’s evolving regulatory landscape and develop strategies to support successful drug development across diverse markets. This Masterclass is also Module 25 of the MSc programme.LondonUnited KingdomM2525O
03/03/2026Drug Device Combinations and Other TechnologiesGain the knowledge and skills to navigate the complex regulatory landscape for innovative medical technologies, including drug–device combinations and products manufactured using non-traditional processes. This course is also Module 18 of the MSc programme.LondonUnited KingdomMSCMD1826F
03/03/2026Drug Device Combinations and Other TechnologiesGain the knowledge and skills to navigate the complex regulatory landscape for innovative medical technologies, including drug–device combinations and products manufactured using non-traditional processes. This course is also Module 18 of the MSc programme. OnlineMSCMD1826O
10/03/2026Compiling Successful Clinical Trial ApplicationsGain a clear understanding of Clinical Trial Application (CTA) requirements across the EU and beyond, including the latest updates on the EU Clinical Trial Regulation 536/2014 and CTIS. Learn practical strategies for managing CTAs effectively through expert-led, interactive sessions.LondonUnited KingdomCT26F