Pharma Deadline Extended: Govt Grants Relief to Small & Medium Firms

The Ministry of Health & Family Welfare has given three months from February 11, 2025, to the small and medium pharmaceutical firms to submit their plan for upgradation to the central license approving authority in order to be eligible to qualify for Schedule M deadline extension, the ministry said in a release.

The ministry further said it has conditionally extended the due date for implementation of revised Schedule M, the good manufacturing practices provision, in respect of small and medium manufacturers having turnover of Rs 250 crore or less, up to December 31, 2025.

On December 28, 2023, the Centre notified revised ‘Schedule M’ requirements wherein “good manufacturing practices” was upgraded to “good manufacturing practices and requirements of plan and equipment for pharmaceutical products”.

Under this, manufacturers were divided into two groups with the first category of large manufacturers having turnover more than Rs 250 crore. A timeline of six months was given to such manufacturers for compliance and the revised Schedule M requirements have been implemented for these manufacturers from June 28, 2024.

For small and medium manufacturers with turnover less than or equal to Rs 250 crore, a timeline of 12 months was given for compliance.

“Small and medium manufacturers had represented for extension of timeline to enable improvement in infrastructure, training of personnel and arranging financial resources,” the ministry said.

It added, “The same has been considered and the small and medium manufacturers have been given a time of three months from February 11, 2025, to submit their plan for upgradation in Form A to the Central License Approving Authority. For such manufacturers who submit these details, the timeline of implementation would be extended till December 31, 2025.”

The revised Schedule M requirements are a positive step towards ensuring the quality and safety of pharmaceutical products being manufactured in India, the ministry said.

The new regulations would enable the pharma companies to not only strengthen their domestic position but also become more competitive globally, it added.

Source: PTI

Related Posts

  • Pharma
  • March 22, 2025
  • 107 views
SHRC orders criminal proceedings against fake doctor

Thiruvananthapuram:  The state human rights commission (SHRC) chairperson Justice Alexander Thomas has ordered the Medical Council Registrar to initiate criminal proceedings under the Kerala Medical Practitioners Act 2021 against a…

  • Pharma
  • March 22, 2025
  • 117 views
Karnataka home to hundreds of startups in med, pharma sectors: Minister MB Patil

BENGALURU: Karnataka is emerging as a key player in the dermatology and cosmetic medical treatment sectors, with significant investment opportunities coming up, particularly in the upcoming KWIN City project, said…

Leave a Reply

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

You Missed

SHRC orders criminal proceedings against fake doctor

SHRC orders criminal proceedings against fake doctor

Karnataka home to hundreds of startups in med, pharma sectors: Minister MB Patil

Karnataka home to hundreds of startups in med, pharma sectors: Minister MB Patil

Piramal Pharma arm, BrePco Biopharma get UKMHRA approval for Neoatricon in UK

Piramal Pharma arm, BrePco Biopharma get UKMHRA approval for Neoatricon in UK

Medical shop sealed for illegal sale of psychotropic drugs

Medical shop sealed for illegal sale of psychotropic drugs

Popular diabetes drug, Mounjaro, launched in India

Popular diabetes drug, Mounjaro, launched in India

Pharma industry says UK pricing revenue unsustainable, blocking investments

Pharma industry says UK pricing revenue unsustainable, blocking investments