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.

Start dateTitleDescriptionCityCountry
12/05/2025The EU Paediatric RegulationThis Masterclass will enable delegates to understand the legislative framework and practical aspects of the EU Paediatric Regulation and considerations around designing paediatric clinical trials.LondonUnited Kingdom
12/05/2025The EU Paediatric RegulationThis Masterclass will enable delegates to understand the legislative framework and practical aspects of the EU Paediatric Regulation and considerations around designing paediatric clinical trials. Online
21/05/2025Essentials 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. Online
21/05/2025Essentials 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 Kingdom
27/05/2025CRED Managing Lifecycle and Variations EffectivelyRegulatory professionals in industry and agencies spend a significant amount of time on variations, so getting them right is critical. This practical course provides a clear overview of the EU variations regulation, with a focus on grouping and work-sharing procedures. Through real-world examples, this course explores how to navigate the categorisation guidelines and discuss other critical actions needed for effective lifecycle management. Online
27/05/2025CRED Managing Lifecycle and Variations EffectivelyRegulatory professionals in industry and agencies spend a significant amount of time on variations, so getting them right is critical. This practical course provides a clear overview of the EU variations regulation, with a focus on grouping and work-sharing procedures. Through real-world examples, this course explores how to navigate the categorisation guidelines and discuss other critical actions needed for effective lifecycle management.LondonUnited Kingdom
11/06/2025Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment. Online
11/06/2025Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.LondonUnited Kingdom
16/06/2025The Medical Device Introductory CourseThis training course will provide those new to medical device regulatory affairs with an understanding of the regulatory requirements for medical devices in the EU and UK. The Medical Device Introductory Course has been put together by practicing medical device regulatory affairs professionals and is in-demand from senior leaders in regulatory affairs who need to get their teams up to speed on current European medical device regulatory practices.LondonUnited Kingdom
16/06/2025The Medical Device Introductory CourseThis training course will provide those new to medical device regulatory affairs with an understanding of the regulatory requirements for medical devices in the EU and UK. The Medical Device Introductory Course has been put together by practicing medical device regulatory affairs professionals and is in-demand from senior leaders in regulatory affairs who need to get their teams up to speed on current European medical device regulatory practices. Online
24/06/2025CRED Successfully Navigating European GMO RequirementsInnovative products that are genetically modified (GM), such as many advanced therapy medicinal products (ATMPs) and viral vector-based vaccines, are subject to a more complex regulatory environment and requirements are constantly evolving. While the application requirements have become more streamlined for specific product types in recent years, there are still gaps in the knowledge of stakeholders who develop these products which can lead to potential delays in drug development. This course explains regulatory frameworks and discusses strategies and practical approaches to streamline the drug development pathway for these product types. Online
24/06/2025CRED Successfully Navigating European GMO RequirementsInnovative products that are genetically modified (GM), such as many advanced therapy medicinal products (ATMPs) and viral vector-based vaccines, are subject to a more complex regulatory environment and requirements are constantly evolving. While the application requirements have become more streamlined for specific product types in recent years, there are still gaps in the knowledge of stakeholders who develop these products which can lead to potential delays in drug development. This course explains regulatory frameworks and discusses strategies and practical approaches to streamline the drug development pathway for these product types.LondonUnited Kingdom
08/07/2025CRED Successfully Navigating European Regulatory ProceduresA course designed for individuals involved in developing European regulatory strategies for projects or wishing to gain the knowledge and skills to contribute to regulatory strategies.LondonUnited Kingdom
08/07/2025CRED Successfully Navigating European Regulatory ProceduresA course designed for individuals involved in developing European regulatory strategies for projects or wishing to gain the knowledge and skills to contribute to regulatory strategies. Online
11/07/2025Essentials of In-Vitro Diagnostics Regulatory AffairsThis course will provide a basic, comprehensive grounding in regulatory affairs for IVDs in a relaxed and interactive environment. Online
11/07/2025Essentials of In-Vitro Diagnostics Regulatory AffairsThis course will provide a basic, comprehensive grounding in regulatory affairs for IVDs in a relaxed and interactive environment.LondonUnited Kingdom
22/07/2025CRED Medical Product Regulation in the UK Part 1A new comprehensive training course, given by experts, who will provide an insight into the evolving regulatory requirements for the development, approval, and distribution of medical products in the United Kingdom (UK).  This is Part 1, covering medicines and medicine-device combinations.LondonUnited Kingdom
22/07/2025CRED Medical Product Regulation in the UK Part 1A new comprehensive training course, given by experts, who will provide an insight into the evolving regulatory requirements for the development, approval, and distribution of medical products in the United Kingdom (UK).  This is Part 1, covering medicines and medicine-device combinations. Online
22/07/2025Sponsored Webinar-Transforming Regulatory ProcessesFREE SPONSORED WEBINAR - This webinar will provide an overview of regulatory intelligence and the typical questions that a regulatory professional receives during the course of the product life cycle.  How the information requests are typically addressed, including information sources, and then how both free and for a fee AI tools can be utilized, including the validity of the output and time savings, will be discussed. Online
23/07/2025US Regulation of Medical DevicesThis Masterclass will provide you with a comprehensive understanding of the US regulatory procedures for medical devices, to enable you to make recommendations about regulatory strategy for the US market.LondonUnited Kingdom
23/07/2025US Regulation of Medical DevicesThis Masterclass will provide you with a comprehensive understanding of the US regulatory procedures for medical devices, to enable you to make recommendations about regulatory strategy for the US market. This Masterclass is also Module 21 of the MSc. Online
30/07/2025Regulatory Environment in the Middle East and North AfricaThis Masterclass provides regulatory affairs professionals with a comprehensive introduction to the evolving regulatory landscape in the Middle East and North Africa (MENA). Designed to deepen your understanding of regional frameworks and operational requirements, this course explores the unique challenges and opportunities across MENA markets. You’ll gain the insights needed to navigate this complex environment and place regional developments within a broader global context.LondonUnited Kingdom
30/07/2025Regulatory Environment in the Middle East and North AfricaThis Masterclass provides regulatory affairs professionals with a comprehensive introduction to the evolving regulatory landscape in the Middle East and North Africa (MENA). Designed to deepen your understanding of regional frameworks and operational requirements, this course explores the unique challenges and opportunities across MENA markets. You’ll gain the insights needed to navigate this complex environment and place regional developments within a broader global context. Online
06/08/2025Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.LondonUnited Kingdom
06/08/2025Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.Online 
02/09/2025CRED Getting the CMC Dossier RightThis course workshop led by agency and industry experts will provide an insight into the preparation and management of the pharmaceutical (CMC) information in Module 3 of the regulatory dossier. This course will focus on synthetic molecules.LondonUnited Kingdom
02/09/2025CRED Getting the CMC Dossier RightThis course workshop led by agency and industry experts will provide an insight into the preparation and management of the pharmaceutical (CMC) information in Module 3 of the regulatory dossier. This course will focus on synthetic molecules.Online 
08/09/2025Design Development and Certification of Medical DevicesThis Masterclass will help you to gain an understanding of the design, manufacturing and quality management requirements for product development, the importance and concepts of risk management and the ways in which risk is managed from the design stage onwards, so that you can provide appropriate advice on the key regulatory issues affecting design, certification and manufacturing of medical devices. Online
08/09/2025Design Development and Certification of Medical DevicesThis Masterclass will help you to gain an understanding of the design, manufacturing and quality management requirements for product development, the importance and concepts of risk management and the ways in which risk is managed from the design stage onwards, so that you can provide appropriate advice on the key regulatory issues affecting design, certification and manufacturing of medical devices.LondonUnited Kingdom
16/09/2025Regulatory Requirements for Cell Tissue & Gene TherapiesModule 22 of the MSc and Masterclass: Designed for regulatory affairs professionals to develop and deepen their understanding of all aspects of the regulation of advanced therapy medicinal products, which has grown in significance over the past five years. It fills a gap in the educational needs for contemporary regulatory affairs specialists. It will allow students to examine the regulatory requirements for advanced therapy medicinal products in the EU and compare this with other territories. It will consider the scientific principles underpinning the development and regulation of advanced therapy medicinal products and the complexities involved.LondonUnited Kingdom