The Commission for Air Quality Management recently directed that all end-of-life vehicles (ELV) will not be given fuel in ...

Under the proposed amendments, entities seeking to validate mobile numbers will be required to pay Rs 3 per validation request. The system will operate through a new Mobile Number Validator (MNV) ...

India's markets regulator on Tuesday proposed to increase the board oversight of key exchange functions, including the ones ...

The PRIP scheme aims to boost India's pharmaceutical R&D by facilitating applications for innovative med tech.

Learn how in vitro diagnostic (IVD) devices can comply with IVDR and Indian MDR standards, ensuring regulatory alignment, ...

The black boxes will provide cockpit conversations and data related to the plane's engine and control settings to ...

As the use of medical device software and software as a medical device (SaMD) grows, regulatory bodies around the world are ...

CCTV Security: India's stringent new surveillance regulations spark conflict with CCTV manufacturers, citing national security fears regarding Chinese technology. The rules require testing of all ...

India's medical device exports increased to ₹ 1,015.02 crore in 2023-24 from ₹ 897.41 crore in the year before, while imports surged to ₹ 2,295.37 crore from 1,682.14 crore. (Reuters) ...

According to the Department of Pharmaceuticals' annual report for 2024-25, India imported medical devices worth $8.1 billion, while exports stood at $3.7 billion in the financial year 2023-24 (FY24) ...

CE marking, representing the pinnacle of safety and performance, is an indispensable requirement for medical devices intended for sale within the European Union and jurisdictions adhering to the EU ...

A steep 27% US tariff threatens India’s medical device exports, but regulatory hurdles may pose an even bigger challenge. Can India secure fairer trade terms and retain its foothold in a ...