Regulatory affairs courses, webinars, conferences and events

We offer a comprehensive programme of training courses and conferences 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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5/29/2019TOPRA In Scotland MeetingThe next TOPRA in Scotland meeting will be held from 14:00 until 17:00 on 29 May 2019 and hosted by Precision for Medicine, Oncology and Rare Disease in Edinburgh.United KingdomSC29MAY19
5/29/2019Regulation of Electrical, Electronic and Software DevicesThis Masterclass will enable you to understand the practical and strategic regulatory issues relating to the development, maintenance and marketing of active devices. It will enable you to critically debate the commercial implications and the impact of the regulations on product stakeholders. (This course is also Module 20 of the TOPRA MSc Regulatory Affairs.)United KingdomMSCM2019
5/30/2019Webinar: Introduction To Data VisualisationThis webinar will provide an introduction to the latest data visualisation techniques being used to get the most insight from scientific and clinical data. How you visualise scientific and clinical data can powerfully influence the insights gained, conclusions drawn and the decisions that are made. This webinar can help you make the most of your data and ensure you aren’t missing important insights that could be used to support your internal decision making processes or your regulatory approvals.OnlineWEBDATA19
6/5/2019Webinar: GMDN Primer for Regulatory Affairs ProfessionalsGet an understanding of Global Medicinal Device Nomenclature (GMDN) and how this can be best managed.OnlineWEBGMDN19
6/5/2019Collaborating with the World: Open Source ScienceThis exclusive TOPRA Fellow evening will be held at TOPRA HQ in London. Prof Matthew Todd, Chair of Drug Discovery at University College London, will explain Open Source Science and its uses.United KingdomFELJUNE19
6/6/2019Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic, comprehensive grounding in regulatory affairs in a relaxed and interactive environment.BelgiumBAS0619
6/12/2019Managing Lifecycle and Variations EffectivelyRegulatory professionals in industry and agency spend a significant amount of time  on variations, so getting them right is critical.United KingdomVAR19
6/12/2019TOPRA In Ireland MeetingJoin the next TOPRA In Ireland Member meeting with talks covering Digital Transformation in Regulatory Affairs and a roundtable discussion on regulatory interactions in emerging markets, East Asia and other regions.IrelandIREJUNE19
6/19/2019Compiling Successful Clinical Trial ApplicationsThis course will equip you with the key knowledge on Clinical Trials applications you need as a regulatory professional.United KingdomCT19
6/25/2019Regulatory Intelligence: How to do it wellAs the amount of information available and the complexity of the regulatory field are ever-increasing, the importance of the regulatory intelligence function grows as well. This Roundtable will provide a focused look at its benefits, challenges and approach.United KingdomRTJUNE2019
7/3/2019Regulatory Strategy for a New Active Substance: NonclinicalThis 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. This is also Module 2 of the TOPRA MSc Regulatory Affairs.United KingdomMSC22019
7/9/2019Essentials of European Medical Device Regulatory AffairsThis course will provide a basic, comprehensive overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.United KingdomMEDBAS319
7/10/2019The 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.United KingdomINTROMD19
7/23/2019Webinar: Product Development for the Japanese MarketThis webinar will discuss product development stages for the Japanese market. WEBJAPAN19
8/5/2019Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic, comprehensive grounding in regulatory affairs in a relaxed and interactive environment.United KingdomBAS0819
9/5/2019Webinar: Improving Writing for PatientsIn today's day and age, giving people usable information about their treatments has never been so important, as such, it is vital to know how to write and present this information. Attend this webinar learn the best way to communicate with patients. WEBSMPC19
9/11/2019Getting 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.United KingdomCMC19
9/19/2019Critically Evaluating DossiersThis course will help you critically analyse dossiers by understanding the importance of helping the assessor find pivotal information, as well as the importance of having consistent messages across Module 2, and between the summaries and the documents of Module 3-5.United KingdomDOSS19
9/25/2019US 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. Additionally it will provide you with an understanding of a globally important market in addition to the knowledge of the EU that the rest of the course provides.This is also Module 21 of the MSc Regulatory Affairs.United KingdomMSCM212019
9/26/2019Webinar: Quality/CMC Considerations for ATMPsThis webinar will provide an overview of the quality/CMC considerations with respect to clinical trial applications and marketing applications for advanced therapy medicinal products (gene and cell therapy products). This will include an outline of the current guidance for these product types for the EU and the USA and specific challenges for cell-based therapies, gene therapies and combined ATMPs.OnlineWEBATMPCMC
9/30/2019Veterinary Medicines Symposium 2019The Veterinary Medicines Symposium will concentrate on how we can improve animal health with veterinary medicines by looking at how we collaborate now and in the future, what strategies could be put in place and how we can work together towards new solutions.IrelandVETSYM2019
9/30/2019Human Medicines Symposium 2019Speakers from agencies across Europe will provide a broad range of insight and facilitate discussion into the world of regulatory affairs on matters affecting industry professionals today and in the future.IrelandSYM2019
9/30/2019TOPRA Annual Symposium Exhibitor Package 2019A truly unique and valuable event in regulatory affairs – the only conference entirely focused on healthcare regulatory affairs allowing you to meet a closely defined group of professionalsIrelandSYMEXHIB19
10/1/2019Medical Devices/IVDs Symposium 2019The regulation of medical devices is continually changing as more innovative technologies and drug-device combinations are being developed. Anyone involved in medical devices and in vitro diagnostics needs to keep up to date with both the new EU regulations and the clinical requirements.IrelandMDSYM2019
10/2/2019Regulatory Updates for SMEsDesigned for small to medium-sized enterprises (SMEs), our 2019 regulatory update is a one-day event which will take place on 2 October in parallel with TOPRA's 2019 Annual Symposium.IrelandSME2019
10/16/2019Essentials of European Medical Device Regulatory AffairsThis course will provide a basic, comprehensive overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.United KingdomMEDBAS219
10/17/2019Regulatory Update: Veterinary Variations in the EUThis is a comprehensive overview of how to prepare and submit variations to VMP marketing authorisations. It provides an update on the latest changes and advice on best practice for experienced regulatory professionals.United KingdomVETVAR19
11/5/2019The Autumn Introductory CourseOur annual Autumn Introductory course is a comprehensive 4-day introduction to EU Pharmaceutical Regulatory Affairs (also Module 0 of the MSc Regulatory Affairs programme).GermanyIC219
11/20/2019Data Management and Digitalisation in Regulatory AffairsThis Masterclass will provide you with  the theoretical background to data management, document management, electronic submissions, eCompliance regulatory information management and the new identification of Medicinal Products (IDMP) requirements, and find solutions to practical problems in this area. Deal with large volumes of data and deal with different data (from nonclinical to post-market pharmacovigilance.  This is also Module 12 of the TOPRA MSc Regulatory Affairs.United KingdomMSCM122019
11/28/2019Essentials of European Pharmaceutical Regulatory AffairsThis course will provide a basic, comprehensive grounding in regulatory affairs in a relaxed and interactive environment.United KingdomBAS1119