Navigating the regulatory landscape for medical devices 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 BfArM. The PEI's mandate encompasses the evaluation of medical equipment for performance and compliance with European Community. Manu… Read More

Entering the medical instrument market in India presents a unique set of challenges and rewards. A crucial first step for any company looking to sell their products within this dynamic landscape is understanding and adhering to the stringent registration process. This process, overseen by the Central Drugs Standard Control Organisation (CDSCO), ver… Read More

The Indian medical device market is booming, presenting a tremendous opportunity for international players. However, navigating the regulations of registration can be challenging. This comprehensive guide will provide you with the essential information needed to effectively register your medical products in India. We will delve into the different r… Read More