Fieldfare Consulting
Quality and regulatory compliance consulting for medical device and in-vitro diagnostics companies
Highlights
- Young companyFounded 2022
- New on EvolcAdded 2026-11-10
About Fieldfare Consulting
Fieldfare Consulting Ltd provides quality and regulatory compliance services for medical devices and in-vitro diagnostics. Services cover quality management systems (ISO 13485, ISO 27001), lean procedure documentation for ISO 13485, ISO 27001, IEC 62304 and ISO 14971, regulatory affairs including CE marking and technical files, and staff training from roundtable discussions to classroom sessions.
Clients are medical device and in-vitro diagnostics companies, from early-stage businesses to established manufacturers. The firm sells consulting engagements and training packages.
The company was founded in 2022 and is registered in Newmarket, United Kingdom. Its director and principal consultant has over 15 years of experience in quality assurance and regulatory affairs for medical devices and diagnostics.
Product: Quality management system documentation, regulatory affairs and CE marking support, technical files, and compliance training packages.
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