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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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
26/05/2022Sponsored: The future of electronic product informationFREE SPONSORED WEBINAR  - An open conversation on the challenges of medicines safety information distribution in Europe and the future of electronic product information. OnlineSPOWEBDP22
07/06/2022CRED 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 Medical Device Regulations on MAAs which came into effect in May 2021?  - This course will explain the current stage of developments as MAHs prepare for the new requirements. OnlineDRUG22O
07/06/2022CRED 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 Medical Device Regulations on MAAs which came into effect in May 2021?  - This course will explain the current stage of developments as MAHs prepare for the new requirements.BrusselsBelgiumDRUG22
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
14/06/2022CRED 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 KingdomCOMM0622
21/06/2022Sponsored: how regulators view Human Challenge Trial resultsFREE SPONSORED WEBINAR - From breakthrough designation to pivotal efficacy data: how are global regulators looking at Human Challenge Trial results? OnlineSPOWEHV22
23/06/2022Essentials of In-Vitro Diagnostics Regulatory AffairsThis course will provide a basic, comprehensive grounding in regulatory affairs for IVDs in a relaxed and interactive environment. OnlineIVDBAS22O
23/06/2022Essentials 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 KingdomIVDBAS22
28/06/2022CRED Managing Lifecycle and Variations EffectivelyRegulatory professionals in industry and agencies spend a significant amount of time on variations, so getting them right is critical.LondonUnited KingdomVAR22
28/06/2022CRED Managing Lifecycle and Variations EffectivelyRegulatory professionals in industry and agencies spend a significant amount of time on variations, so getting them right is critical. OnlineVAR22O
05/07/2022The 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.WatfordUnited KingdomINTROMD
05/07/2022The Medical Device Introductory Course Online(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. OnlineINTROMD2
04/08/2022Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic but comprehensive overview of pharmaceutical regulatory affairs in a relaxed and interactive environment.LondonUnited KingdomBAS040822
01/09/2022CRED Understanding Digital Health and Electronic ProductsRegulation on electrical, electronic and software medical devices.LondonUnited KingdomEE22
01/09/2022CRED Understanding Digital Health and Electronic ProductsRegulation on electrical, electronic and software medical devices.Online EE22ONLINE
05/09/2022Post-Market Surveillance and Vigilance for Medical DevicesThis Masterclass is also Module 16 of the MSc Regulatory Affairs and will help to define the terminology and explain the concepts of vigilance and post-market surveillance, their practical applications and integration into the life cycle of a medical device. This course will focus on meeting European requirements.LondonUnited KingdomMD162022
05/09/2022Post-Market Surveillance and Vigilance for Medical DevicesThis Masterclass is also Module 16 of the MSc Regulatory Affairs and will help to define the terminology and explain the concepts of vigilance and post-market surveillance, their practical applications and integration into the life cycle of a medical device. This course will focus on meeting European requirements. OnlineMSCM1622O
14/09/2022Veterinary Medicines Regulation Update: Product InformationThis workshop will cover the legislative requirements and practicalities imposed by the new regulation on packaging and labelling, and will offer an opportunity for discussion with industry professionals and regulators. OnlineWVETREG
20/09/2022CRED An Overview of Regulatory Product InformationThis one day workshop from regulators and industry experts will provide an insight on European SmPC, package leaflet (PL) and label preparation and implementation, from a strategic and practical point of view.Online SMPC0922O
20/09/2022CRED An Overview of Regulatory Product InformationThis one day workshop from regulators and industry experts will provide an insight on European SmPC, package leaflet (PL) and label preparation and implementation, from a strategic and practical point of view.LondonUnited KingdomSMPC22
21/09/2022CRED 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 PM0922O
21/09/2022CRED 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 KingdomPM22
05/10/2022CRED 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 CM2210O
05/10/2022CRED 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 KingdomCMC22
12/10/2022Regulatory Strategy for Established Active SubstancesThis Masterclass is also Module 7 of the MSc and is designed for regulatory affairs professionals to develop and deepen their understanding of all aspects of the regulation of and the strategic issues to be considered in relation to medicines containing established active substances, including line extensions, generics and the relevant aspects for OTC products. It will allow them to examine the regulatory requirements imposed on these substances.LondonUnited KingdomMSCM72022
12/10/2022Regulatory Strategy for Established Active SubstancesThis Masterclass is also Module 7 of the MSc and is designed for regulatory affairs professionals to develop and deepen their understanding of all aspects of the regulation of and the strategic issues to be considered in relation to medicines containing established active substances, including line extensions, generics and the relevant aspects for OTC products. It will allow them to examine the regulatory requirements imposed on these substances. OnlineMSCM72022O