CDSCO issues Draft Guidance Document on Conduct of Medical Device Software under MDR 2017
by Mahek Sancheti on 2025-10-30
The Central Drugs Standard Control Organisation (CDSCO) has released a draft guidance document for manufacturers and importers of medical device software.
List of Standards Published under Medical Equipment and Hospital Planning (MHD) of BIS- 2025
by Parul Bohral on 2025-10-29
Medical technology and hospital infrastructure significantly shape the way modern healthcare operates today. To ensure the safety, reliability, and quality of medical devices, the Bureau of Indian Standards (BIS) established the Medical Equipment and Hospital Planning Division (MHD).
Electronics Components Manufacturing Scheme (ECMS): Driving India's Electronics Future
by Mahek Sancheti on 2025-10-28
The government has approved the first seven projects under the Electronics Components Manufacturing Scheme (ECMS). These projects are worth ₹5,532 crore and are expected to produce goods worth ₹44,406 crore.
Environment Ministry Revised White Category Industries under the Air and Water Acts
by Mahek Sancheti on 2025-10-27
The Ministry released two new rules under the Air and Water Acts. These rules include a fresh list of White Category industries.
CDSCO Circular for Online Pharmacies on GST Cuts for Medicines and Devices
by Mahek Sancheti on 2025-10-27
The Ministry of Health and Family Welfare has revised the Goods and Services Tax (GST) rates for medicines, pharmaceuticals, and medical devices. The new GST structure came into effect on 22 September, which aims to lower the price of essential medicines and equipment.
What Indian Wholesalers & Retailers Should Know About Exporting FDA-Regulated Pharmaceuticals and Medical Devices to the U.S.
by Parul Bohral on 2025-10-27
India is a significant exporter of pharmaceuticals and medical devices worldwide, with the U.S. being a crucial marketplace. For wholesalers and retailers, exporting to the U.S. can be profitable, but it requires strict adherence to FDA regulations.