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
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…
Audit & Certification
Information Security
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Standards & Schemes
ISO 9001 Quality Management Systems
ISO 9001 Quality Management Systems ISO 9001 provides a robust framework that can be tailored to any industry or sector. It offers a systematic and…
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
Program for Endorsement of Forest Certification (PEFC)
Program for Endorsement of Forest Certification (PEFC) The PEFC (Program for Endorsement of Forest Certification) provides an assurance mechanism for purchasers of wood and paper…
Audit & Certification
Forestry
Forestry Forest management and sustainability strive to balance the economic, social, and environmental dimensions of forest use Purchasing decisions for forestry-related raw materials and end-of-line…