EPR Authorization Amendment: Step-by-Step Overview
by Parul Bohral on 2025-10-31
An EPR Authorization Amendment is an official modification made to an existing EPR certificate issued by the Central Pollution Control Board (CPCB).
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).
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.
CDSCO Issues Circular on Recent Changes to GST Rate Structure for Zonal Offices
by Parul Bohral on 2025-10-23
The Central Drugs Standard Control Organization (CDSCO) has recently issued a circular to all its Zonal and Sub-Zonal Offices. It concerns the implementation of the revised GST rate structure for medicines, medical devices, and related healthcare products.
Revised GST Rate Structure for Chemists and Druggists
by Parul Bohral on 2025-10-21
The government recently updated the GST rate structure for chemists and druggists. These revisions directly affect how GST applies to various medicines, healthcare products, and related services.
Separate Provision for Subsequent Importer in the CDSCO Online System
by Parul Bohral on 2025-10-16
The Central Drugs Standards Control Organization (CDSCO) has been transforming the regulatory framework for medical devices in India.