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Tim LAWTON

Position:	Principal consultant
Company/Institution:	C-REG Medical
Location/Metro Area:	France, Marseille
Languages Spoken:	English , French
Discipline:	Engineering
Focus:	Biomedical devices and instrumentation
Qualified as a Manufacturing Systems Engineer, I gained a wide engineering experience as a Production / Industrial Engineer, Production Manager and Quality Assurance Manager in the UK. Arrived in France in 1996, gained experience as a QA Manager, specialising as a Regulatory Affairs Manager for both medical device and in-vitro device manufacturers. In 2006, I created C-REG Medical : a Complete REGulatory Affairs Service. Fluent in French & English, I assist small medical device manufacturers in their Regulatory obligations to your requirements, for both Europe and the USA. Please feel free to consult the website : www.c-reg-medical.com

Public Profile: Link to your full profile from blogs and sites.
http://www.labroots.com/app/account/profile_view/Tim.LAWTON

Education

From:

Sep 1987

To:

Jun 1991

Degree:

Technical Degree

Institution:

University of Hertfordshire

Field of Study:

BEng (HONS), Manufacturing Systems Engineering

Work Experience

From:

Sep 2006

To:

Present

Company:

C-REG Medical

Type of Business:

Regulatory Affairs / Quality Assurance consulting for medical device manufacturers

Title:

Director / principal consultant

From:

Nov 2001

To:

Sep 2006

Company:

HoribaABX (now Horiba Medical)

Type of Business:

Medical device manufacturer : in-vitro diagnostics

Title:

Regulatory Affairs Manager

From:

Jun 1996

To:

Oct 2001

Company:

Diagnostic Medical Systems

Type of Business:

Medical device manufacturer

Title:

Quality Assurance / Regulatory Affairs

My Research

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Articles in Refereed Journals

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Presentations Webinars, Speeches, Lectures, Video

Dissertations and Theses

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Courses Taught