Basic info
Industry
business consulting and services
Sectors
Medical Device
Internal Audits
EU 2017/745
Medical Device Classification
Jargon Free
UKCA Marking
CE Marking
External Audits
Technical File Writing
ISO 14971
ISO 13485
EU Medical Device Regulatory Affairs
Medical Device Compliance
Person Responsible for Regulatory Compliance
ISO 10993
Quality Management Representative
UK Responsible Person
Health Care
ISO 9001
Consulting
Medical
Biological Evaluation Report
Quality Assurance
Medical Device Regulations
Date founded
2017