Let us unravel your COMPLIANCE issues
Phone for a free no obligation quote on 07774 857622
What Can MDC Offer You?
We offer a range of services in Quality, Regulatory, Technical & Compliance within the Medical Device arena including New Product Development, Lean Initiatives, Problem Solving, Supply Chain Management, Business Improvement Tools, Quality Tools, Quality Remediation, Internal & External Auditing, CAPA, Product Evaluation, KPI’s, Cost Of Quality, Project and Environmental Management, Due Diligence, Public and Product Liability Claims, CE marking, Product Compliance, Market Applications and Submissions, CFR 820 requirements, Homologation applications, Product recalls, Third Party Testing and EU representation.
decipher and understand Directives, Standards & Legislation.
One phone call or email to Simon gives me the answers I need or the support I require, to ensure my Business Compliance objectives are met.
Adverse Incident & Vigilance reporting
Product & System Standards
Product Regulatory Assessment
Third Party Testing
CE Marking & Technical File Compliance
Post Market Surveillance
EU Authorised Representative
LEGAL & TECHNICAL
Product Liability Claims
Advisory Capacity On EC Directives
Advisory Capacity On UK Statutes
Advisory Capacity On Contractual Issues
New Product Development & Integration
Product Life Cycle Analysis
Customer/Supplier Visits & Audits
Due Diligence (Acquisitions)