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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:

Client Services
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Quality Management Systems Inspiring the confidence of customers and staff, gain greater transparency, and drive high-performance outcomes. Adopting a Quality Management System that instills a…
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StandardsMark™ Download
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IATF 16949 – Automotive Quality Management System
IATF 16949 – Automotive Quality Management System IATF 16949:2016 helps your automotive organization reduce variation and waste in the supply chain using continuous improvement. IATF…
Product Certification
Gas Safety Certification Scheme
Gas Safety Certification Scheme QCI Global offers Gas Safety Certification for gas appliances and components. QCI Global’s Gas Appliances and Components Scheme is a type…
Standards & Schemes
AS 9110 Aerospace Certification
AS 9110 Aerospace Certification The requirements for personnel conducting Maintenance, Repair, and Overhaul (MR&O) tasks is crucial for ensuring the competence and qualification of your…

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