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Home
Consultancy Services
UK
UK Responsible Person
Medical Device Regulatory Consultancy
Auditing Services
Biological Evaluation
Cosmetics Responsible Person
CE Mark & UKCA Mark Technical Files
Clinical Evaluation
ISO 13485 QMS
PPE Authorised Representative
Europe
EU Authorised Representative
Medical Device Regulatory Consultancy
Auditing Services
Biological Evaluation
Cosmetics Responsible Person
CE Mark & UKCA Mark Technical Files
Clinical Evaluation
ISO 13485 QMS
PPE Authorised Representative
USA
FDA 510(k) Submissions
FDA Device Exemption
FDA QSR Consulting
QSR Audits
FDA Medical Device Classification
FDA Pre-Submissions
FDA 483 Warning Letters
US FDA Medical Device Services
Medical Device Testing
About Us
Blogs
Contact us
Software Tools
EU MDR Medical Device Classification Tool
EU MDR Medical Device Determination Tool
EU Medical Device Regulatory Roadmap
David Small