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.

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.

Data pager
Data pager
12
 Page 1 of 2, items 1 to 30 of 52.
Show all 52
Start dateTitleDescriptionCityCountry
Data pager
Data pager
12
 Page 1 of 2, items 1 to 30 of 52.
Show all 52
29/05/2024CRED Managing Lifecycle and Variations EffectivelyRegulatory professionals in industry and agencies spend a significant amount of time on variations, so getting them right is critical. OnlineLCM24
29/05/2024CRED Managing Lifecycle and Variations EffectivelyRegulatory professionals in industry and agencies spend a significant amount of time on variations, so getting them right is critical.RotterdamNetherlandsLCMF2F24
31/05/2024Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.RotterdamNetherlandsMBAS0824
31/05/2024Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.Online BAS0824O
05/06/2024Strategic Planning in Regulatory AffairsModule 1 of the MSc and Masterclass: This Masterclass will help you understand the practical and strategic aspects of global regulatory affairs, and enable you to develop your knowledge and skills to provide advice to your company to help develop a regulatory strategy.LondonUnited KingdomMSCM12024
05/06/2024Strategic Planning in Regulatory AffairsModule 1 of the MSc and Masterclass: This Masterclass will help you understand the practical and strategic aspects of global regulatory affairs, and enable you to develop your knowledge and skills to provide advice to your company to help develop a regulatory strategy. OnlineMSCM12024O
12/06/2024Essentials 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 MDB0624O
12/06/2024Essentials 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.London MDBAS0624
12/06/2024Regulatory Careers Live 2024 - Belgium In-PersonRegulatory Careers Live is 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.BrusselsBelgiumRCLBRUSS24
12/06/2024TOPRA in Scotland - Medical Devices & In Vitro DiagnosticsTOPRA in Scotland would like to invite members and non-members to a presentation on Medical Devices and In Vitro Diagnostics.EdinburghUnited KingdomSCOJUN24
18/06/2024The Regulatory Landscape for Medical Device InnovationsThe TOPRA Roundtable programme has been designed to enable regulatory affairs professionals to discuss their challenges and learn from each other’s experiences in industry and agencies. They offer the chance to be part of a unique learning experience which will enable you to contribute to lively debates and develop action plans that you can implement in your organisation with confidence.LondonUnited KingdomRTAPR242
18/06/2024The Regulatory Landscape for Medical Device InnovationsThe TOPRA Roundtable programme has been designed to enable regulatory affairs professionals to discuss their challenges and learn from each other’s experiences in industry and agencies. They offer the chance to be part of a unique learning experience which will enable you to contribute to lively debates and develop action plans that you can implement in your organisation with confidence. OnlineRTAPR242O
26/06/2024The 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.LondonUnited KingdomMDINTRO24
02/07/2024Joint Regulatory and HTA Advice: Getting Ready for 2025The TOPRA Roundtable programme has been designed to enable regulatory affairs professionals to discuss their challenges and learn from each other’s experiences in industry and agencies. They offer the chance to be part of a unique learning experience which will enable you to contribute to lively debates and develop action plans that you can implement in your organisation with confidence.LondonUnited KingdomRTAPR243
03/07/2024Essentials of In-Vitro Diagnostics Regulatory AffairsThis course will provide a basic, comprehensive grounding in regulatory affairs for IVDs in a relaxed and interactive environment.OnlineOnlineIVDB24O
03/07/2024Essentials 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 KingdomIVDB24
09/07/2024CRED 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 KingdomERP24
09/07/2024CRED 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. OnlineERPON24
17/07/2024Regulatory Control of Clinical OperationsThis Masterclass is also Module 5 of the MSc and will provide you with an understanding of the practical and regulatory aspects of global clinical research, in order to offer effective advice on the regulatory issues likely to arise during clinical programmes. OnlineMSCM524O
17/07/2024Regulatory Control of Clinical OperationsThis Masterclass is also Module 5 of the MSc and will provide you with an understanding of the practical and regulatory aspects of global clinical research, in order to offer effective advice on the regulatory issues likely to arise during clinical programmes.LondonUnited KingdomMSCM52024
06/08/2024Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.Online BAS0824ON
06/08/2024Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.LondonUnited KingdomBAS0824F
04/09/2024CRED 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 KingdomCMCF2F24
09/09/2024Registering Biological Biotech & Advanced Therapy ProductsModule 9 of the MSc and Masterclass: Designed for regulatory affairs professionals to develop and deepen their understanding of all aspects of the regulation and scientific principles underpinning development of biological, biotechnology and advanced therapy products, which provide challenges with their inherent complexities. The module includes consideration of the data requirements for clinical trial applications and marketing applications.Online MSCM92024O
09/09/2024Registering Biological Biotech & Advanced Therapy ProductsModule 9 of the MSc and Masterclass: Designed for regulatory affairs professionals to develop and deepen their understanding of all aspects of the regulation and scientific principles underpinning development of biological, biotechnology and advanced therapy products, which provide challenges with their inherent complexities. The module includes consideration of the data requirements for clinical trial applications and marketing applications.LondonUnited KingdomMSCM924F
11/09/2024Regulatory Careers Live 2024 - UK In-PersonRegulatory Careers Live is 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.LondonUnited KingdomRCL24UK
17/09/2024CRED Understanding Digital Health and Electronic ProductsRegulation on electrical, electronic and software medical devices. OnlineUDHON24
24/09/2024CRED Successful and Skilful CommunicationSkilful communication and negotiation skills are essential for effective regulatory professionals. Learn to recognise and use different negotiation strategies whilst maintaining trust and respect with complex groups of stakeholders. Develop and deliver impactful presentations and documents that deliver the results you need.LondonUnited KingdomSSCS24
25/09/2024CRED An Overview of Regulatory Product InformationThis one-day workshop with expert speakers from health authorities and industry will give you an understanding of the strategic development of the regulatory product information in Europe and UK. From company core data sheet to Summary of Product Characteristics (SmPC), Labelling and the Package Leaflet (PL). This is a hands-on workshop covering not just the theoretical approach to creating product information in Europe, but also includes practical exercises for the preparation and implementation of Labelling. You will also hear an overview on what in the pipeline on future digital advancements for labeling.LondonUnited KingdomSMPC24F2F
25/09/2024CRED An Overview of Regulatory Product InformationThis one-day workshop with expert speakers from health authorities and industry will give you an understanding of the strategic development of the regulatory product information in Europe and UK. From company core data sheet to Summary of Product Characteristics (SmPC), Labelling and the Package Leaflet (PL). This is a hands-on workshop covering not just the theoretical approach to creating product information in Europe, but also includes practical exercises for the preparation and implementation of Labelling. You will also hear an overview on what in the pipeline on future digital advancements for labeling.Online SMPC24O