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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02/02/2022Regulatory Requirements for a New Active Substance: QualityThis Masterclass is also Module 3 of the TOPRA MSc Regulatory Affairs and will help you understand and provide advice on quality data requirements in the pharmaceutical regulatory environment as well as address practical regulatory questions in this area.CheshamUnited KingdomMSC32022
02/02/2022Regulatory Requirements for a New Active Substance: QualityThis Masterclass is also Module 3 of the TOPRA MSc Regulatory Affairs and will help you understand and provide advice on quality data requirements in the pharmaceutical regulatory environment as well as address practical regulatory questions in this area. OnlineMSCM32022O
08/02/2022Essentials 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 KingdomVETBAS22
08/02/2022Essentials 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. OnlineVETBAS22O
15/02/2022CRED Regulatory Document Writing and ManagementSkills based course on the theory and practice of writing regulatory documents and communications for optimal impact and effectiveness.LondonUnited KingdomDOC22
15/02/2022CRED Regulatory Document Writing and ManagementSkills based course on the theory and practice of writing regulatory documents and communications for optimal impact and effectiveness. OnlineDOC22O
23/02/2022CRED European IVD Regulatory AffairsThis two and a half day interactive course will cover all the key topics and areas of responsibility for professionals taking on the Person Responsible for Regulatory Compliance role under the IVDR. It will also provide comprehensive information for anyone responsible for implementing the necessary changes to be ready when the IVDR comes into force.LondonUnited KingdomIVD222
23/02/2022CRED European IVD Regulatory AffairsThis two and a half day interactive course will cover all the key topics and areas of responsibility for professionals taking on the Person Responsible for Regulatory Compliance role under the IVDR. It will also provide comprehensive information for anyone responsible for implementing the necessary changes to be ready when the IVDR comes into force. OnlineIVD222O
15/03/2022CRED 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. OnlineERP2022O
15/03/2022CRED 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.BrusselsBelgiumERP22
17/03/2022Essentials of European Pharmaceutical Regulatory AffairsThis course will provide an overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.LondonUnited KingdomBAS170322
17/03/2022Essentials of European Pharmaceutical Regulatory AffairsThis course will provide an overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.Online BAS170322O
23/03/2022Design, Development and Certification of Medical DevicesThis Masterclass is also module 14 of the MSc Regulatory Affairs and 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 KingdomMD1422
23/03/2022Design, Development and Certification of Medical DevicesThis Masterclass is also module 14 of the MSc Regulatory Affairs and 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. OnlineMSC142022O
28/03/2022The 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. OnlineIC12022
27/04/2022CRED IVD Regulatory Affairs for Global MarketsIncrease your impact as a regulatory professional and expand your IVD expertise beyond Europe with this two and a half day course.LondonUnited KingdomIVDGM22
27/04/2022CRED IVD Regulatory Affairs for Global MarketsIncrease your impact as a regulatory professional and expand your IVD expertise beyond Europe with this two and a half day course. OnlineVIVD221
04/05/2022Essentials 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.LondonUnited KingdomMDBAS22F2F
04/05/2022Essentials 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. OnlineMDBAS22O
10/05/2022Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.BrusselsBelgiumBAS0522
10/05/2022Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment. OnlineBAS0522O
16/05/2022Regulatory Strategy for a NAS: Global Clinical DevelopmentRegulatory Strategy for a New Active Substance: Global Clinical Development  is also Module 4 of the MSc and will help you to understand and develop regulatory strategies for all aspects of global clinical research, as well as address practical regulatory issues in this area.BrusselsBelgiumMSCM42022
16/05/2022Regulatory Strategy for a NAS: Global Clinical DevelopmentRegulatory Strategy for a New Active Substance: Global Clinical Development  is also Module 4 of the MSc and will help you to understand and develop regulatory strategies for all aspects of global clinical research, as well as address practical regulatory issues in this area. OnlineMSCM42022O
19/05/2022CRED 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 KingdomCOMM0522
23/05/2022Clinical Evaluation of Medical DevicesThis Masterclass is also Module 15 of the MSc Regulatory Affairs and will help you to understand the broad scope of clinical investigation and the regulatory processes required with the alternative routes to demonstrate compliance.LondonUnited KingdomMSCMD1522
23/05/2022Clinical Evaluation of Medical DevicesThis Masterclass is also Module 15 of the MSc Regulatory Affairs and will help you to understand the broad scope of clinical investigation and the regulatory processes required with the alternative routes to demonstrate compliance. OnlineMSMD1522O
31/05/2022CRED Regulation of Drug Device Combination ProductsAre you developing new pharmaceutical products? Do they include (or are they provided with) any type of administration device?  If yes, are you fully aware of the impact of the new Medical Device Regulations on MAAs from May 2020?  - This course will explain the current stage of developments as MAHs prepare for the new requirements.BrusselsBelgiumDRUG22
31/05/2022CRED Regulation of Drug Device Combination ProductsAre you developing new pharmaceutical products? Do they include (or are they provided with) any type of administration device?  If yes, are you fully aware of the impact of the new Medical Device Regulations on MAAs from May 2020?  - This course will explain the current stage of developments as MAHs prepare for the new requirements. OnlineDRUG22O
08/06/2022Regulatory 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 KingdomMSCM520222
08/06/2022Regulatory 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. OnlineMSCM522O