DEUTSCHLAND CDSCO: REGULATORY LANDSCAPE FOR MEDICAL DEVICES

Navigating the regulatory landscape for medical equipment in Germany can be a complex process. The primary regulatory authority responsible for overseeing this domain is the Paul-Ehrlich-Institut, commonly known as the Bundesinstitut für Arzneimittel und Medizinprodukte. The PEI's mandate encompasses the assessment of medical equipment for efficac

Importing medical devices into India requires a thorough understanding of the regulatory landscape and a meticulous adherence to established procedures. This step-by-step manual aims to demystify the process, outlining the key requirements, regulations, and documentation needed for a smooth import of medical devices into the Indian market. ,To be