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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 course covers all aspects of the product development process, and provides a sound overview of EU legislation and regulatory procedures, including the central role regulatory affairs plays in modern healthcare companies.
When: November 3–5, 2026
Where: London
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This course covers all aspects of the product development process, and provides a sound overview of EU legislation and regulatory procedures, including the central role regulatory affairs plays in modern healthcare companies.
When: November 3–5, 2026
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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 will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.
When: September 22, 2026
Where: Online
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This course will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.
When: September 22, 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
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 course will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.
When: May 1, 2026
Where: London
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This course will provide an overview of regulatory requirements and considerations for medical devices in a relaxed and interactive environment.
When: May 1, 2026
Where: Online
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This course covers all aspects of the product development process, and provides a sound overview of EU legislation and regulatory procedures, including the central role regulatory affairs plays in modern healthcare companies.
When: April 14–16, 2026
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This course covers all aspects of the product development process, and provides a sound overview of EU legislation and regulatory procedures, including the central role regulatory affairs plays in modern healthcare companies.
When: April 14–16, 2026
Where: London
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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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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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