Germany's regulatory framework for health products is a complex and rigorous system. Companies seeking to sell their products in Germany must meet the stringent standards set forth by the Central Drugs Standard Control Organisation (CDSCO). These regulations cover a wide scope of aspects, including product safety, labeling, and production. A dee… Read More

India's healthcare sector is witnessing rapid development. This situation has driven a boom in the demand for advanced medical devices. However, companies seeking to launch these instruments in India must adhere to a detailed registration framework. The registration pathway for medical devices in India is regulated by the Central Drugs St… Read More

The healthcare device industry in India is experiencing rapid growth. This presents both thrills and rewards. To participate successfully, manufacturers need to conform with the stringent regulations set by the Central Drugs Standard Control Organization (CDSCO). This resource provides a comprehensive overview of the process for registering medi… Read More

In India, the Central Drugs Standard Control Organization (CDSCO) regulates medical devices in accordance with the Medical Device Rules 2017 India. For medical device registration India on the Sugam portal, one essential requirement is the submission of a Plant Master File (PMF). This document provides detailed information about the legal manufa… Read More