All our staff have extensive industrial and, in some cases, regulatory agency experience. We are fully up-to-date with the the very latest international regulatory and GMP compliance requirements and we have the experience to help you implement efficient, cost-effective solutions to your technical and regulatory challenges.
All our staff have extensive industrial and, in some cases, regulatory agency experience. We are fully up-to-date with the the very latest international regulatory and GMP compliance requirements and we have the experience to help you implement efficient, cost-effective solutions to your technical and regulatory challenges.
At NSF-DBA, we pride ourselves on providing the very best technical advice and training available anywhere. We use only top quality, experienced industry professionals to give you the top quality service you need.
Our associates have worked and continue to work for 5 of the top European Notified bodies and have over 30 years combined experience undertaking Technical and Quality management system assessments for European, Canadian, US and other international regulatory systems using the Notified body structure.
Our Medical Devices practice covers a range of capabilities for the changing demands in regulatory and technical requirements. We have a deep technical coverage of Products, Therapy areas, Global Regulations as well as. Our associates are either specialist, world-renowned leaders within their field and / or have the practical experience of doing the things that need to be done. In our training and education services we appreciate the need to “Teach, Support and Coach” therefore we have the appropriate people
Partners
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Mr Martin Lush
Senior Partner
CBiol, MSB, PGDip, FIBMS
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Mr Peter Gough
Partner
MSc, CSci, CChem, FRSC, FCQI, CQP
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Mr Mike Halliday
Partner
BSc (Pharm), MRPharmS, PGDip
Customer Services
Partners
Biomedical scientists
Operations Managers
