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This Masterclass is also Module 6 of the MSc regulatory Affairs and 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. You will 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... Details
When: December 1–3, 2026
Where: London
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This Masterclass is also Module 6 of the MSc regulatory Affairs and 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. You will 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... Details
When: December 1–3, 2026
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This 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.
When: October 13–14, 2026
Where: Online
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This 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.
When: October 13–14, 2026
Where: Online
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This Masterclass is also Module 17 of the MSc Regulatory Affairs (previously know as Regulatory and Related Activities Through the Device Lifecycle) 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... Details
When: October 6–8, 2026
Where: London
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This Masterclass is also Module 17 of the MSc Regulatory Affairs (previously know as Regulatory and Related Activities Through the Device Lifecycle) 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.
When: October 6–8, 2026
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This 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.
When: September 15–16, 2026
Where: London
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This 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.
When: September 15–16, 2026
Where: Online
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Module 9 of the MSc and Masterclass: Designed for regulatory affairs professionals to develop and deepen their understanding of all aspects of the regulation and scientific principles underpinning development of biological, biotechnology and advanced therapy products, which provide challenges with their inherent complexities. The module includes consideration of the data requirements for clinical trial applications and marketing... Details
When: September 8–10, 2026
Where: London
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Module 9 of the MSc and Masterclass: Designed for regulatory affairs professionals to develop and deepen their understanding of all aspects of the regulation and scientific principles underpinning development of biological, biotechnology and advanced therapy products, which provide challenges with their inherent complexities. The module includes consideration of the data requirements for clinical trial applications and marketing... Details
When: September 8–10, 2026
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This 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.
When: July 7–9, 2026
Where: London
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This 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.
When: July 7–9, 2026
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This training course will provide those new to medical device regulatory affairs with an understanding of the regulatory requirements for medical devices in the EU and UK. The Medical Device Introductory Course has been put together by practicing medical device regulatory affairs professionals and is in-demand from senior leaders in regulatory affairs who need to get their teams up to speed on current European medical device regulatory... Details
When: June 2–4, 2026
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This training course will provide those new to medical device regulatory affairs with an understanding of the regulatory requirements for medical devices in the EU and UK. The Medical Device Introductory Course has been put together by practicing medical device regulatory affairs professionals and is in-demand from senior leaders in regulatory affairs who need to get their teams up to speed on current European medical device regulatory... Details
When: June 2–4, 2026
Where: London
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Learn to consider and evaluate the practical regulatory aspects of regulatory strategy and data requirements for abridged applications (generics), specialised products (herbals, drug-device combination, radiopharmaceuticals, cosmetics, inhalation and blood products) and strategic issues of abridged US options.
When: May 19–21, 2026
Where: London
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Learn to consider and evaluate the practical regulatory aspects of regulatory strategy and data requirements for abridged applications (generics), specialised products (herbals, drug-device combination, radiopharmaceuticals, cosmetics, inhalation and blood products) and strategic issues of abridged US options.
When: May 19–21, 2026
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This Masterclass 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. This Masterclass is also Module 16 of the MSc Regulatory Affairs
When: April 28–30, 2026
Where: London
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This Masterclass 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. This Masterclass is also Module 16 of the MSc Regulatory Affairs
When: April 28–30, 2026
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The 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 authorisations for veterinary medicinal products.
When: March 17, 2026
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According to Investors in People, poor leadership and management costs UK business around £85 billion per year in lost productivity alone. This course will help you to prevent such costs within your organisation by helping you to manage improved performance, engagement and retention.
When: January 28, 2026
Where: London
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This 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 impaally debate the commercial implications and the impact of the regulations on product stakeholders.
When: December 2–4, 2025
Where: London
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This 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 Masterclass is also Module 20 of the MSc.
When: December 2–4, 2025
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Join us at Plaisterers' Hall, London on 27 November for the Awards for Regulatory Excellence to celebrate the achievements of individuals, teams and organisations in the regulatory affairs community.
When: November 27, 2025
Where: London
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