Medical Devices
Medical devices are instruments, equipment, implants, or software used in the diagnosis, treatment, or prevention of medical conditions
he regulatory requirements for the medical devices industry have become more complex in recent years, primarily aimed at ensuring patient safety and protecting the end consumer.
Meet Regulatory Requirements While Protecting Consumers Safety
Meeting regulatory requirements and protecting consumer safety are critical objectives for the medical devices industry
Related Services
In addition to the services mentioned earlier, there are several related services that can further support improving business excellence maturity and sustainable business practices. These services include:
Standards & Schemes
FSSC 22000 Standard
FSSC 22000 FSSC 22000 (Food Safety System Certification 22000) is a globally recognized food safety certification scheme. It provides a framework for effectively managing food…
Client Services
Non-Conformance Processes
Non-Conformance Processes QCI Global Assurance personnel, services, decisions, and clients Definitions Non-conformance processes are an integral part of quality management systems and are designed to…
Sector
Aerospace
Aerospace Confidence and trust in the aerospace industry is vital for the success of businesses operating within this sector. Given the critical nature of aerospace…
Audit & Certification
Why Certify
Why Certify Certification provides a range of benefits that contribute to the success and growth of organizations. Drive Continuous Improvement Encourage employees at all levels…
Standards & Schemes
RC 14001 – Responsible Care
RC 14001 – Responsible Care While ISO 14001 focuses on environmental matters, the RC 14001 scope expands to address companies effectively manage health, safety, and…
Standards & Schemes
e-Stewards® Standard
e-Stewards® Standard The e-Stewards Standard for Responsible Recycling and Reuse of Electronic Equipment. The e-Stewards® Standard has been designed to serve recyclers, re-furbishers, asset managers,…