Regulatory affairs courses, webinars, conferences and meetings

We offer a comprehensive programme of training courses, conferences, meetings and webinars on a wide range of regulatory affairs topics.

Our courses 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.

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06/05/2025CRED Project Management for Regulatory Affairs ProfessionalsA two-day, skills-based course on the theory and practice of managing project teams to produce optimal regulatory documents and communications for those working in the pharmaceutical industry.LondonUnited KingdomPMF2F25
06/05/2025CRED Project Management for Regulatory Affairs ProfessionalsA two-day, skills-based course on the theory and practice of managing project teams to produce optimal regulatory documents and communications for those working in the pharmaceutical industry. OnlinePMO25
06/05/2025Sponsored Webinar-Innovative Medical DevicesFREE SPONSORED WEBINAR - This webinar will provide valuable insights into the challenges and opportunities in the MedTech regulatory landscape. OnlineSPWBSI25
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 KingdomM230525F2F
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. OnlineM230525O
13/05/2025Meet Representatives of the Belgian Agency, FAMHPMembers of the TOPRA IN Benelux Community Steering Group are pleased to invite you to a webinar during which representatives of the Belgian Federal Agency of Medicines and Healthcare Products (FAMHP) will present the current organisation and the key activities on which the Agency is focussing in line with its strategic business plan. The webinar will cover the key three divisions of the Agency: Directorate General (DG) Pre-Authorisation, DG Post-Authorisation and DG Inspection. OnlineBENMAY25
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. OnlineMDBAS0625
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 KingdomMDBAS11
22/05/2025Regulatory News - Pharmaceuticals / Medical DevicesThis evening is an excellent opportunity to hear the latest regulatory news for pharmaceuticals and medical devices. We will discuss the ongoing work with the revision of pharmaceutical legislation in Europe, information on update of the variation regulation and experiences with MDR and IVDR implementation. We also get to hear the latest about TOPRA. Open to anyone working with and interested in regulatory questions for pharmaceuticals and medical devices SwedenSWEMAY25
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. OnlineLCMO25
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 KingdomLCMF2F25
10/06/2025What Regulatory Professionals Should Know About the HTARThe TOPRA In Benelux Community Steering Group is pleased to present this webinar sharing the most important elements of the Health Technology Assessment Regulation (HTAR) in Europe for regulatory professionals. OnlineBENJUN25
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. OnlineBAS0625ONL
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 KingdomBAS0825O
13/06/2025Regulatory Careers Live 2025 - Brussels, BelgiumRegulatory Careers Live is Europe’s only careers fair dedicated to healthcare regulatory affairs. It is free to attend and your opportunity to meet with potential future employers and get essential advice from some of the most respected and influential leaders in the field of regulatory affairs.BrusselsBelgiumRCL25BRU
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 KingdomMDINTRO25
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. OnlineMDINTRO25O
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. OnlineGMO25
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 KingdomGMO25F2F
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 KingdomERP25
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. OnlineERP25O
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. OnlineIVB25O
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 KingdomIVDB25
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 KingdomCREDUKMPR
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. OnlineCREDUKMPRO
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 KingdomMSCM2125
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. OnlineMSCM2125O
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 KingdomM240725F2F
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. OnlineM24300725O
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 KingdomBAS0825