This certification specifies requirements for a quality management system for medical device manufacturers. It demonstrates that a company has implemented a quality management system
CE Marking
This marking is a requirement for medical devices sold in the European Union. It indicates that a product meets the safety, health, and environmental protection requirements of the EU.
GMP Certification
This certification demonstrates that a manufacturer follows Good Manufacturing Practices (GMP) to ensure the quality and safety of their products.
The Surgical Instruments Manufacturers Association of Pakistan
