Labeling Requirements for Registration of Medical Devices in India
Medical Device manufacturers must follow the labeling requirements and must be done on every medical device packaging. An overview of the process for registration of medical devices in India here. The CDSCO is the Indian FDA which handles all regulations for medical devices in India. On 25th September, 2014 the CDSCO issued amendments to the Drugs and Cosmetics Rules, 1945. An important […]
“Come Make in India” – Stunning First Visit PM Modi in the US
This article narrates PM Modi’s visit to US stressing Make in India campaign and what it means to the Life Science Sector. FDI & IP: Key Takeaways for the Life Science Industry following the Indian PM Narendra Modi’s first visit to the US Considered to be one of the most auspicious times in the Hindu […]
Registration of Medical Devices in India
This article talks about the overall process of registration of medical devices in India. At the federal government level, medical device registration is processed by the Central Drug Standards Control Organisation (CDSCO) under the Ministry of Health and Family Welfare. Manufacturers can leverage their approvals in the US, Canada, Europe, Australia or Japan to comply […]