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
ISO 45001 Occupational Health and Safety Management System
ISO 45001 Occupational Health and Safety Management System ISO 45001 is an international standard that specifies the requirements for an occupational health and safety management…
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…
Audit & Certification
Information Security
Information Security Information and cybersecurity, refers to the practices and measures taken to protect digital information from unauthorized access, use, disclosure, disruption, modification, or destruction.…
Client Services
StandardsMark™ Download
5 Ticks StandardsMark™ Download Promote your certification by displaying the 5 Ticks StandardsMark™ from QCI Global. Select from the drop-down menu items listed below, and…
Sector
Manufacturing & Engineering
Manufacturing & Engineering ISO certification can indeed provide an immediate boost to an organization’s credibility and reputation, giving them a competitive edge in the market.…