Regulatory affairs conferences and courses

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
2/27/2018Essentials of European Medical Device Regulatory AffairsThis one-day course will give you a comprehensive overview of regulatory requirements and considerations for medical devices.MEDBAS18
2/28/2018Post-Market Surveillance and Vigilance for Medical DevicesModule 16 of the MSc (Medical Devices) and Masterclass. To define the terminology and explain the concepts of vigilance and post-market surveillance, their practical applications and integration into the lifecycle of a medical device. The focus is on meeting European requirements.MC162018
3/6/2018Essentials 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.BAS18
3/13/2018CRED+ Optimising Interactions With RegulatorsThis is a practical workshop covering interactions with EU and US health authorities.ADVICE17
3/21/2018CMC SPIN Webinar: Technical DiscussionTOPRA CMC SPIN is pleased to introduce this free members-only interactive technical webinar which will be held on 21 March 2018 from 2-4 pm GMT.CMCMARCH18
3/22/2018CRED 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 enable you to contribute to regulatory strategiesERP18
4/11/2018The US Regulatory EnvironmentModule 11 of the MSc (Medicines) and Masterclass: The purpose of this module is to provide you with an understanding of the regulatory environment in the USA in order to place these global influences in perspective. As the largest single country market for pharmaceutical products, the regulatory requirements of the US FDA has a major influence on the design of pharmaceutical development programmes both within the USA and globally. This module offers an understanding of the US regulatory environment in order to place these global influences in perspective.MSCM112018
4/16/2018The Spring Introductory CourseIntroduction to Pharmaceutical Regulatory Affairs (Module 0 of the MSc Regulatory Affairs)IC12018
4/19/2018CRED Demonstrating Appropriate Dosage Form DesignA practical workshop on bioequivalence and biowaivers. This course bridges the gaps between the guidelines and the practicalities as well as the clinical aspects of bioequivalence and the quality/pharmacy aspects of dissolution.BIO18
4/30/2018Regulatory Careers Live LondonRegulatory Careers Live is your opportunity to meet with potential future employers and get essential advice from some of the most respected and influential leaders in the field of regulatory affairs.CAREERS18
5/14/2018Essentials 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.BAS0518
5/21/2018CRED Getting the CMC Dossier RightThis two-day workshop led by regulators and industry experts will provide an insight into the preparation and management of the pharmaceutical (CMC) information within the regulatory dossier.CMC18
5/30/2018Regulatory Strategy for Established Active SubstancesModule 7 of the MSc (Medicines) and Masterclass: This module is designed for regulatory affairs professionals to develop and deepen their understanding of all aspects of the regulation of 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.MSCM72018
6/6/2018Regulatory Careers Live DublinAn opportunity to meet with potential future employers and get essential advice from some of the most respected and influential leaders in the field of regulatory affairs.CAREEIRE18
6/7/2018CRED Managing Variations EffectivelyVariations are core to lifecycle maintenance and vital to ensure a product registration is up to date. This practical CRED workshop will explain the principles of the EU Variations Regulation. This workshop will cover also intricacies of procedures for grouping and worksharing, and use examples to illustrate the guidelines on categorisation.VAR18
6/13/2018Introduction To Medical Device Regulation in Europe(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.INTROMD18
6/21/2018Essentials of European Medical Device Regulatory AffairsHeld in Ireland, this one-day course and will provide a comprehensive overview of regulatory requirements and considerations for medical devices.MEDBAS218
6/27/2018CRED Understanding Clinical DevelopmentThis two-day workshop will provide an overview with practical advice from regulators and industry on the process of designing and conducting clinical trials from phase I through phases II, III and even clinical trials considerations beyond drug marketing approval.CD18
8/1/2018CRED Project Management for Regulatory Affairs ProfessionalsA two-day course providing an essential overview of project management relating specifically to regulatory affairs professionals.PM18
8/3/2018Essentials 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.BAS0818
9/3/2018Drug 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
9/26/2018Regulatory Strategy From Development To the Market PlaceModule 6 of the MSc: This 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 life-cycle 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
10/1/2018Human Medicines SymposiumSpeakers 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
10/1/2018Medical Devices SymposiumThe 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 requirementsMDSYM2018
10/2/2018Veterinary SymposiumThe 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 solutionsVETSYM2018
10/11/2018CRED 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
10/24/2018Regulatory and related activities throughout the device lifeModule 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
11/14/2018CRED Compiling Successful Clinical Trial ApplicationsThis workshop based course will equip you with the key regulatory knowledge on Clinical TrialsCT18
11/22/2018Essentials 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
11/28/2018Data 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 for abridged applications and specialised products, and explore and critically debate the regulatory issues likely to arise in order to be able to provide effective advice on such situations.MSCM82018
Join Now