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.
How to Obtain a CGWA Compliance Report
by Parul Bohral on 2025-10-15
A CGWA Compliance Report is an official document that businesses, industries, infrastructure projects submit to get permission from the Central Ground Water Authority when they plan to extract groundwater.
Telecommunications Network Authorisation Rules 2025: Complete Guide to Categories, Eligibility, Application Process and Compliance
by Mahek Sancheti on 2025-10-14
The Telecommunications (Authorisation for Telecommunication Network) Rules are a proposed legal framework that would be made under the powers granted by sections 3 and 56 of the Telecommunications Act, 2023.
‘Not of Standard Quality’: Coldrif Banned in States after Death of Children in MP
by Mahek Sancheti on 2025-10-13
In October 2025, 14 children died in Madhya Pradesh, India. Investigations revealed that all of the children had suffered acute kidney failure and that they had consumed a cough syrup called Coldrif.
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RCMC Export Promotion Council for Medical Devices (EPC)
by Parul Bohral on 2025-10-10
The Registration-cum-Membership Certificate (RCMC) is an official registration granted to exporters by an authorized Export Promotion Council (EPC) or Commodity Board under the Foreign Trade Policy (FTP) of India.
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Hazardous Waste Authorization Annual Return: Filing, Compliance & Legal Requirements
by Parul Bohral on 2025-10-09
The Hazardous Waste Authorization Annual Return is a legal requirement under the Hazardous and Other Wastes (Management and Transboundary Movement) Rules, 2016.