Auditing & Monitoring for Compliance and Improvement
With you we maintain and develop of your QMS and product certification with cost effective, independent, thorough Auditing & Monitoring Processes to
- Assess compliance with Regulations / Standards, your QMS and Technical Documentation and
- Identify improvements and efficiencies.

Providing efficient, cost effective services using experienced, qualified Auditors who can;
Design, collate and maintain an efficient Auditing & Monitoring Schedule / Plan
Perform Internal Audit, Supplier, Contract Manufacturer, Fulfilment / Distribution audits at planned intervals or as stand-alone service, to monitor compliance and identify where improvements and efficiencies can be realised
Conduct monitoring of Post Market Surveillance, Vigilance, PMCF and Medical Device Reporting
Prepare Reports and as appropriate Corrective & Preventive Actions (CAPA)

Design / Develop
Risk Management
Audit & Monitor
Technical
Documentation
Change Control
Clinical Evaluation
Data Analysis
Doc & Data Control
Launch & Distribute
Management
Systems
NCR & CAPA
Ops Management
Performance Improvement
Regs & Standards
Reg Strategy & Plan
Reg Submission
Verification & Validation
Vigilance & PMS