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:
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…
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…
Standards & Schemes
Costco Supplier Requirements
Costco Supplier Requirements All facilities that are involved in processing, packing, warehousing, or distributing consumable products or supplying food-contact packaging materials to Costco Wholesale Corporation…
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
Responsible Recycling© (R2)
R2v3 – The Sustainable Electronics Reuse & Recycling (R2) Standard V3 The practice of refurbishing, de-manufacturing, recycling, and reusing electronics can pose various health and…
