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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29/11/2022Essentials of European Medical Device Regulatory AffairsThis face-to-face course will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.DublinIrelandMDBAS22
29/11/2022Essentials of European Medical Device Regulatory AffairsThis online course will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment. OnlineMDBAS1122
30/11/2022Regulatory Strategy From Development To the MarketplaceThis Masterclass is also Module 6 of the MSc regulatory Affairs and will enable you to consider and evaluate the practical regulatory aspects of regulatory strategy for commercialising products and maintaining the brand from the development stages to registration and throughout the product lifecycle. You will explore and critically debate the regulatory issues likely to arise prior to and during commercialising of products in order to be able to provide effective advice on such situations. OnlineMSCM62022O
06/12/2022Sponsored: Post-Market Surveillance requirementsFREE SPONSORED WEBINAR - Post-Market Surveillance requirements for Medical Devices and IVDs OnlineSPOWEQBD22
13/12/2022Sponsored: Future Trends on European Medicines RegulationsFREE SPONSORED WEBINAR - Future Trends on European  Medicines Regulations OnlineSPOWEBVT22
15/12/2022Sponsored: The evolving environment of Regulatory AffairsFREE SPONSORED WEBINAR - The evolving environment of Regulatory Affairs - insight in career path of regulatory professionals at Roche OnlineSPWROCNO22
24/01/2023CRED 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 KingdomCOMM231
01/02/2023US Regulation of Medical DevicesModule 21 of the MSc and Masterclass - This course 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 KingdomMSCM2123
01/02/2023US Regulation of Medical DevicesModule 21 of the MSc and Masterclass - This course 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.  MSCM2123O
07/02/2023Compiling Successful Clinical Trial ApplicationsThis face-to-face course will equip you with the key knowledge on Clinical Trials applications you need as a regulatory professional.BrusselsBelgiumCT23
07/02/2023Compiling Successful Clinical Trial ApplicationsThis course will equip you with the key knowledge on clinical trials applications you need as a regulatory professional.OnlineOnlineCT23O
22/02/2023Essentials of European Veterinary Regulatory AffairsThe world of veterinary regulatory affairs can be a confusing and complex place, particularly if you have no formal veterinary or regulatory affairs background. The purpose of this course is to provide you with a clear and concise understanding of the role played by regulatory affairs in obtaining and maintaining marketing authorisation for veterinary medicinal products.LondonUnited KingdomVETBAS23
22/02/2023Essentials of European Veterinary Regulatory AffairsThe world of veterinary regulatory affairs can be a confusing and complex place, particularly if you have no formal veterinary or regulatory affairs background. The purpose of this course is to provide you with a clear and concise understanding of the role played by regulatory affairs in obtaining and maintaining marketing authorisation for veterinary medicinal products.Online VETBAS23O
07/03/2023CRED 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 KingdomERP23
15/03/2023Regulatory Strategy for a New Active Substance NonclinicalModule 2 of the MSc and Masterclass: This Masterclass will give delegates an understanding of the practical and legislative requirements for the nonclinical phase of global drug development. It will explore the regulatory issues that are likely to arise and provide advice and discussion around solutions to such situations.  MSCM223O
15/03/2023Regulatory Strategy for a New Active Substance NonclinicalModule 2 of the MSc and Masterclass: This Masterclass will give delegates an understanding of the practical and legislative requirements for the nonclinical phase of global drug development. It will explore the regulatory issues that are likely to arise and provide advice and discussion around solutions to such situations.LondonUnited KingdomMSCRAM223
21/03/2023Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.LondonUnited KingdomBAS0323
28/03/2023The Spring Introductory Course (Pharmaceuticals)Module 0 of the MSc:  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.LondonUnited KingdomIC22023P
18/04/2023Regulation of In-Vitro Diagnostics Medical DevicesModule 19 of the MSc and Masterclass: Primarily focusing on the In Vitro Diagnostic Regulation, this course will present the latest information covering the new regulation and how this differs from the In Vitro Diagnostic Directive in the EU and other jurisdictions.LondonUnited KingdomMDM1923
18/04/2023Regulation of In-Vitro Diagnostics Medical DevicesModule 19 of the MSc and Masterclass: Primarily focusing on the In Vitro Diagnostic Regulation, this course will present the latest information covering the new regulation and how this differs from the In Vitro Diagnostic Directive in the EU and other jurisdictions.  MSCM1923O
25/04/2023CRED Regulatory Document Writing and ManagementSkills based course on the theory and practice of writing regulatory documents and communications for optimal impact and effectiveness.LondonUnited KingdomDW23
25/04/2023CRED Regulatory Document Writing and ManagementSkills based course on the theory and practice of writing regulatory documents and communications for optimal impact and effectiveness.OnlineUnited KingdomDW23O
03/05/2023CRED 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.Online PM23O
03/05/2023CRED 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 KingdomPM23
08/05/2023Leadership and Strategic Management in Regulatory AffairsModule 10 of the MSc and Masterclass: This 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.  MSCM1023O
08/05/2023Leadership and Strategic Management in Regulatory AffairsModule 10 of the MSc and Masterclass: This 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.BrusselsBelgiumMSCRAM1023
15/05/2023Registering 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 KingdomMSCM92023
15/05/2023Registering 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.  MSCM923O
23/05/2023CRED Managing Lifecycle and Variations EffectivelyRegulatory professionals in industry and agencies spend a significant amount of time on variations, so getting them right is critical. OnlineLCM23O
25/05/2023Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment. BelgiumBAS0523