New Pharma Rules In India Effective Today: Are MSMEs Ready? What Will Change For The Industry

New Delhi:  The drug companies in India will now have to meet the standard specified in the revised schedule M – as the new rules come into effect, starting today, January 1. Earlier, the pharmaceutical companies had sought an extension in the implementation of new standards. However, the government did entertain the request meaning now “the industry will have to comply with the provisions or face action” a senior government official to ET.
As per the new provision, government can now initiate audits and risk-based inspection to ensure that the standards are being maintained by drug companies.
The industry must now adhere to the newly implemented Schedule M norms, which outline manufacturing practices and standards for premises, plants, and equipment used in pharmaceutical production. These norms include provisions for annual product quality reviews, quality risk management, and a comprehensive pharmaceutical quality system.
Industry leaders previously met with the health minister to request an extension for implementing the revised Schedule M norms, citing challenges such as delays in procuring machinery and upgrading infrastructure. They urged the ministry to give them extra time to ensure the survival of micro, small, and medium enterprises (MSMEs) in the pharmaceutical sector to adjust to the changes.
Schedule M of the Drugs and Cosmetics Rules, 1945, outlines Good Manufacturing Practices (GMP) for pharmaceutical products, including a system for the prompt recall of defective products. The revised Schedule M was notified by the health ministry in January 2024.
Laghu Udyog Bharati (LUB), an RSS affiliate, and the Federation of Pharma Entrepreneurs (FOPE), representing MSME pharma units, also appealed to Health Minister JP Nadda to defer the implementation of the new norms.
Rajesh Gupta, all-India head of pharma at LUB and president of the Himachal Drug Manufacturers Association, said, “We support the government and have initiated awareness seminars, but we need time until December 2026 for infrastructure upgrades.”
He noted that companies are grappling with issues related to loans, machinery procurement, and infrastructure improvements, all of which require time to resolve.

Related Posts

Green or red dot? Your soap, shampoo and toothpaste will now reveal if they’re veg or non-veg

Green dot or red dot? Soaps, shampoos and toothpaste to reveal if they are veg or non-veg That green dot you usually look for on a food packet could soon…

Counterfeit rabies vaccine worth ₹2 lakh seized in Delhi

The Drugs Control Department has seized counterfeit rabies vaccine worth about ₹2 lakh from a firm in Chandni Chowk’s Bhagirath Palace, the Delhi government said on Tuesday. Health Minister Pankaj…

Leave a Reply

Your email address will not be published. Required fields are marked *

You Missed

Green or red dot? Your soap, shampoo and toothpaste will now reveal if they’re veg or non-veg

Green or red dot? Your soap, shampoo and toothpaste will now reveal if they’re veg or non-veg

Counterfeit rabies vaccine worth ₹2 lakh seized in Delhi

Counterfeit rabies vaccine worth ₹2 lakh seized in Delhi

AIIA organises public awareness rally on 11th Ayurveda Day

AIIA organises public awareness rally on 11th Ayurveda Day

UKHSA and University of Oxford scientists uncover genetic changes in the bacteria causing severe Kent meningococcal disease outbreak

UKHSA and University of Oxford scientists uncover genetic changes in the bacteria causing severe Kent meningococcal disease outbreak

‘Broad daylight dacoity’, says Supreme Court on overpricing of essential cancer drugs

‘Broad daylight dacoity’, says Supreme Court on overpricing of essential cancer drugs

CDSCO finds one spurious drug sample in Delhi, 220 NSQs in Aug surveillance

CDSCO finds one spurious drug sample in Delhi, 220 NSQs in Aug surveillance