Our latest COVID-19 information - full Autumn programme of webinars now in place

Alison Wilson

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Alison is an Independent Regulatory Affairs Consultant. Previously Regulatory Affairs Manager for Smith & Nephew Wound Management, she has over 25 years’ experience of regulatory affairs in medicinal products, human tissue products and medical devices. She is a nominated UK expert for ISO (International Standards Organisation) TC150/WG 11 – Tissue Engineered Medical Products and a member of BSI Technical Panel RGM/1 – Regenerative Medicine.

Drug/Device and Device/Drug Combinations in the EU (European Union) and USA Training Course

Drug/Device and Device/Drug Combinations in the EU and USA

24-25 Sep 2020

Practical guidance on borderline Issues and combination products

Pharmaceutical Development of ATMPs Training Course

Pharmaceutical Development of ATMPs

5-6 Oct 2020

This course will provide a comprehensive overview of the regulatory, quality and GMP requirements to consider when developing ATMPs.

Pharmaceutical Development of ATMPs Training Course

Pharmaceutical Development of ATMPs

22-23 Mar 2021

This course will provide a comprehensive overview of the regulatory, quality and GMP requirements to consider when developing ATMPs.

Pharmaceutical Development of ATMPs Training Course

Pharmaceutical Development of ATMPs

29-30 Mar 2021

This course will provide a comprehensive overview of the regulatory, quality and GMP requirements to consider when developing ATMPs.

Drug/Device and Device/Drug Combinations in the EU (European Union) and USA Training Course

Drug/Device and Device/Drug Combinations in the EU and USA

26-27 Apr 2021

Practical guidance on borderline Issues and combination products

Drug/Device and Device/Drug Combinations in the EU (European Union) and USA Training Course

Drug/Device and Device/Drug Combinations in the EU and USA

28-29 Apr 2021

Practical guidance on borderline Issues and combination products

The Medical Device Summer School - From Concept to CE Marking Training Course

The Medical Device Summer School - From Concept to CE Marking

5-9 Jul 2021

*A practical five-day course with interactive workshops - now in its 17th successful year!*

This comprehensive course has been designed to map the processes from device concept to marketing and show how regulatory, quality, clinical and other aspects of device development are joined into a continuous process.

Pharmaceutical Development of ATMPs Training Course

Pharmaceutical Development of ATMPs

4-5 Oct 2021

This course will provide a comprehensive overview of the regulatory, quality and GMP requirements to consider when developing ATMPs.

Pharmaceutical Development of ATMPs Training Course

Pharmaceutical Development of ATMPs

11-12 Oct 2021

This course will provide a comprehensive overview of the regulatory, quality and GMP requirements to consider when developing ATMPs.