Regulatory affairs courses, 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.

Start dateTitleDescription
30/07/2018Essentials of European Pharmaceutical Regulatory AffairsRegulatory affairs can be a complex place, particularly if you have limited experience. Attend this course to get a clear understanding of the roles played by regulatory affairs professionals in obtaining and maintaining marketing authorisation for medicines; learn the key steps involved in developing new pharmaceuticals; and gain an overview of EU regulatory procedures and first insights about the strategies needed to be applied by regulatory affairs professionals to obtain best results for their organisations and stakeholders.BAS0818
31/07/2018TOPRA Summer SchoolAdvance your regulatory career this summer with a two-course bundle, plus receive free access to a pair on-demand webinars for doing so.CREDSUMMER
31/07/2018CRED Practical Document Writing and ManagementA two-day, skills based, course on the theory and practice of writing optimal regulatory documents and communicationsDOC18
02/08/2018CRED Project Management for Regulatory Affairs ProfessionalsA two-day course providing an essential overview of project management relating specifically to regulatory affairs professionals.PM18
06/08/2018Webinar: Feed Additive EfficacyThe regulatory framework, and data required to establish the characterisation, quality, safety and efficacy of the different types of feed additives will be looked at during this webinar.WEBFEED18
03/09/2018Drug-Device Combinations and Other TechnologiesModule 18 of the MSc (Medical Devices) and Masterclass: This module will enable you to consider and evaluate the practical regulatory aspects including the design, development and lifecycle of a medical device product.MC182018
05/09/2018TOPRA In Sweden MeetingThe next TOPRA In Sweden Networking event will focus on new regulations for medicinal products and medical devices. Attend this meeting as a member for free or join as a guest with our special offer to gain practical tips on the topic on medical trials and medical devices within regulatory affairs.TISSEP2018
07/09/2018CRED Advances in BiotechnologyThis course will provide an insight and overview on the new developments in biotechnology.BIOTECH18
11/09/2018Webinar: Updates on China Regulatory ReformThis is an update on China's recent regulatory reform from 2017. In the past 12 month, more draft regulations/guidelines have been finalised and gone into the implementation stage, which will change China's role in global drug development. Therefore, it is important to follow up to those changes, in order to fully explore China drug development potential.WEBCHINA2
11/09/2018Webinar: Global Development Series OfferTHREE-FOR-TWO OFFER: Explore the world of regulatory affairs with TOPRA's Global Development webinar series.WEBOFFER
20/09/2018CRED Electrical, Electronic and Software Medical DevicesThis course is designed to explain and illustrate the regulatory requirements of electrical, electronic, and software related devices.EE18
26/09/2018Regulatory Strategy From Development To the Market PlaceModule 6 of the MSc: This masterclass module 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 and 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.MSCM62018
01/10/2018Medical Devices Symposium 2018 (Stockholm)The 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.MDSYM2018
01/10/2018Human Medicines Symposium 2018 (Stockholm)Speakers from across the industry 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.SYM2018
02/10/2018Veterinary Symposium 2018 (Stockholm)The Veterinary 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.VETSYM2018
03/10/2018Regulatory Update for Small To Medium-Sized EnterprisesDesigned for small to medium-sized enterprises (SMEs), our 2018 regulatory update is a one-day event which will take place on 3rd October.SME2018
11/10/2018CRED Writing Effective 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.SMPC18
16/10/2018Webinar: EU Nutrition and Health Claim Regulation for FoodsThis webinar will provide an understanding of the dossier requirements for the nutrition and health claims scientific assessment undertaken by the European Food Safety Authority (EFSA).WEBNUTRITI
24/10/2018Regulatory Strategy in the Post Market PhaseModule 17 of the MSc: This is the MSc module 'Regulatory Strategy in the Post-Market Phase'. It will provide regulatory affairs professionals with insight into the strategic issues affecting the commercial and regulatory maintenance of a medical device throughout its lifecycle, with focus on post-launch activities and future pressures.MC172018
31/10/2018Optimising Regulatory Development From Cradle To GraveOptimising regulatory development from cradle to grave - Ensuring the needs of special populations are met.SPECPOP18
06/11/2018Autumn Introductory Course 2018A standalone introduction to Pharmaceutical Regulatory Affairs (also Module 0 - 7FHH1097 of the MSc Regulatory Affairs programme).IC218
14/11/2018CRED Compiling Successful Clinical Trial ApplicationsThis workshop based course will equip you with the key regulatory knowledge on Clinical TrialsCT18
22/11/2018Essentials of European Pharmaceutical Regulatory AffairsRegulatory Affairs can be confusing and complex, particularly if you have no formal industry background. This course provides an awareness of the regulatory environment.BAS1118
28/11/2018Data for Abridged Applications and Specialised ProductsModule 8 of the MSc: This module will enable you to consider and evaluate the practical regulatory aspects of regulatory strategy and data requirements for abridged applications (generics), specialised products (herbals, drug/device combination, radiopharmaceutics, cosmetics, inhalation and  blood products) and strategic issues of  abridged US options.MSCM82018