Consultancy services in the areas of:
 - Medical Device Regulatory Affairs
 - In Vitro Diagnostic Regulatory Affairs
 - Quality Management (ISO 13485:2016)
 - Risk Management (ISO 14971:2019)
 - EU, UK, US, APAC, LATAM device registrations
 - Clinical Affairs
 - Technical Documentation
 - Regulatory Strategy
 - Device Classification
 - Clinical Evaluation Plan/Report
 - Performance Evaluation Plan/Report
 - State of the Art Plan/Report
 - Analytical Performance Plan/Report
 - Clinical Performance Plan/Report
 - Scientific Validity Plan/Report
 - Biological Evaluation Plan/Report

Call or message for more information on services and to arrange a friendly call to discuss the specific needs of your business

Clinical Trials

Consulting

Health Services

Medical Devices

BaxMed Regulatory Ltd

BaxMed Regulatory Ltd's headquarters in Leeds, United Kingdom

Description

People (2)

Stuart Baxter

Nichola Price

Jobs