Industry groups want a joint FTA advisory body to address regulatory hurdles and dumping risks as India negotiates trade deals with the US, EU and UK
BHISHM cubes, the indigenous portable modular medical facility, are being deployed at prominent hospitals such as AIIMS Jammu and SKIMS Srinagar near India's border under the government's Aarogya Maitri project to bolster medical readiness, officials said on Friday. The development comes on the heels of Union Health Minister J P Nadda on Friday reviewing health infrastructure preparedness across hospitals in the country amid the ongoing Operation Sindoor and the ongoing India-Pakistan military conflict, official sources said. These BHISHM cubes are also being stationed in other Institutes of National Importance (INIs) across India, including AIIMS in Rishikesh, Bilaspur and Delhi, they said. "We are also providing operational training to the respective medical institutes where BHISHM cubes have been deployed. So far two BHISHM cubes have been deployed at AIIMS, Jammu and more are being diverted to this centre. "Besides, around 35 other BHISHM cubes so far have been deployed across
Poly Medicure posted a 34 per cent rise in Q4 net profit to Rs 91.8 crore, with revenue up 16.6 per cent, driven by strong export performance and new business verticals
The Indian medical device industry faces challenges from international trade dynamics, regulatory barriers, and domestic policy inconsistencies
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)
The new tariffs may impact India's medical devices exports, said Rajiv Nath, forum coordinator for the Association of Indian Medical Device Industry (AiMeD)
Medtech manufacturers' groups expect negotiations may lead to fairer outcomes for both sides
Move comes even as domestic medtech manufacturers lobby asked GOI to work towards a fair deal
Implementation of tracking system, independent advisory board, lateral entry among panel's recommendations to remove CDSCO's perception of licence raj
Zydus will file a mandatory cash tender offer for the remaining shares of Amplitude at the same purchase price of €6.25 per share
Releases draft format for adverse events for rapid identification and rectification of potential device failures
European conformity assessment firm says it will bring in 'rigorous quality and safety standards'
Health Ministry to constitute expert committee, import suspended until policy framework is finalised
CDSCO to initiate workshops; industry says step will bring regulatory uniformity
A parliamentary committee on Monday raised serious concerns about the country's capability to test and regulate radiation-emitting medical devices, urging immediate reforms in the national testing infrastructure. The Standing Committee on Consumer Affairs, Food and Public Distribution revealed significant gaps in the testing framework for critical medical equipment like X-ray and MRI machines in its fifth report submitted to Parliament. The National Testing House (NTH) currently lacks the expertise and capacity to comprehensively test and certify radiation-emitting medical devices, despite existing regulatory oversight from the Atomic Energy Regulatory Board (AERB) and the Central Drugs Standard Control Organization (CDSCO). The committee recommended establishing a collaborative framework between NTH, AERB, and CDSCO to address the identified regulatory shortcomings. Key recommendations include developing specialised testing capabilities at NTH, investing in advanced testing ...
OneSource Specialty Pharma recently raised Rs 801 crore through equity issuance
Company eyes Rs 30 crore revenue in first year, Rs 200 crore by 2030
CII's medtech group to ask govt for strict policy on import of refurbished devices, incentives in R&D, and enhanced rebate on export duties
The Bureau of Indian Standards (BIS) on Monday said it is prioritising development of standards for 214 critical medical devices, which are set for phased completion by December 2025. These devices, which include septal closure devices, plasma sterilizers, and phototherapy machines, are in line with the National Medical Device Policy, 2023 and have been identified in consultation with Department of Pharmaceuticals. BIS, in a statement, said the national standards body is developing standards for innovative products such as therapeutic footwear, portable ramps, braille displays, and fall detectors, which support individuals with disabilities. BIS has published over 1,700 standards for the medical sector, covering specialities such as cardiology, neurology, orthopaedics, ophthalmology, and more. Of these, around 1,200 standards specifically focus on medical devices critical to healthcare. BIS standards in this sector ensure that Indian medical devices are safe, effective, and globall
A super top-up health insurance plan pays the policyholder for medical expenses that exceed the coverage limit of their base health insurance policy