Medical Device Rules Archives - Medical Device Registration | CDSCO Certificate Consultancy

Post-Market Surveillance in ISO 13485

What is Post-Market Surveillance in ISO 13485?

ISO 13485 is the quality management system that maintains the quality of medical devices in India. So, if you are dealing with

Definition Of Medical Device As Per MDR 2017

Definition of Medical Device As Per MDR 2017

Medical Devices are widely used in all branches of medicine, surgery and community not only in India but across the globe. To

Importance of Medical Device Compliance In India

Importance Of Medical Device Compliance In India

Those dealing with medical devices must understand the importance of medical device compliance in India. This will ensure the medical device’s safety

Documents Required For Medical Device Registration

Documents Required For Medical Device Registration

If you are willing to apply for an MD License in India then you must understand first which license you require. After