Let us unravel your COMPLIANCE issues

Phone for a free no obligation quote on 07774 857622

We are an EU Authorised Representative that offers a range of services in Quality, Regulatory, Technical & Compliance within the Medical Device arena including New Product Development, Supply Chain Management, Business Improvement Tools, Quality Remediation, Internal & External Auditing, CAPA, KPI’s, Cost Of Quality, Project Management, CE marking, Product Compliance, Market Applications and Submissions, CFR 820 requirements, Product recalls and Third Party Testing.

Utilising the resource of M D C Consultancy Ltd allows me to take a proactive approach in the complex world of Regulation without having to read,
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.

Chris Fullerton

Managing Director, Silk Mobility

REGULATORY

Adverse Incident & Vigilance reporting
Product & System Standards
Product Regulatory Assessment
Third Party Testing
Product Recalls
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
Lean Initiatives
Poka Yoke
Problem Solving