Stephen Willmor Email & Phone Number | Over 18 years experience in regulatory affairs in generic pharmaceutical companies with primary focus on European markets but with some experience of US and Rest of the World. Expert in review and authoring of module 3 (CMC) documentation especially Drug Master Files / Active Substance Master Files. Have spent most of my career working with solid oral dosage forms (immediate and modified release) but have experience with nebulisers, eye drops, sterile parenteral products and topical products. Spent some time as regulatory compliance manager so have working knowledge of Good Manufacturing Process (GMP) and audits. Have worked on and alongside clinical experts so knowledge of requirements for bioequivalence / biowaivers is good and have a working knowledge of device regulations especially for combination products.

Stephen Willmor

Over 18 years experience in regulatory affairs in generic pharmaceutical companies with primary focu...
United Kingdom

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Stephen Willmor’s Email swillmor@nemaura.co.uk

Stephen Willmor’s Phone Numbers +44 1509 22****

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Stephen Willmor’s Location United Kingdom

Stephen Willmor’s Current Industry Alturix

Stephen Willmor’s Prior Industry Nemaura Pharma | Teva Pharmaceuticals | Arrow Generics

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Regulatory Affairs Manager At Alturix Limited

2021-06-01 00:00:00 - Present

Regulatory Affairs Manager

2017-11-01 00:00:00 - 2021-06-01 00:00:00

Senior Manager

2011-10-01 00:00:00 - 2017-10-01 00:00:00

Senior Regulatory Affairs Officer And Compliance Manager

2003-04-01 00:00:00 - 2011-09-01 00:00:00

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Stephen Willmor is a Over 18 years experience in regulatory affairs in generic pharmaceutical companies with primary focus on European markets but with some experience of US and Rest of the World. Expert in review and authoring of module 3 (CMC) documentation especially Drug Master Files / Active Substance Master Files. Have spent most of my career working with solid oral dosage forms (immediate and modified release) but have experience with nebulisers, eye drops, sterile parenteral products and topical products. Spent some time as regulatory compliance manager so have working knowledge of Good Manufacturing Process (GMP) and audits. Have worked on and alongside clinical experts so knowledge of requirements for bioequivalence / biowaivers is good and have a working knowledge of device regulations especially for combination products.