Amid Covid battle, drug cos get green breather from govt

New Delhi: Amid continued threat of Covid-19 pandemic and possibility of its third wave, the Centre has exempted drug manufacturers from stringent environmental clearance processes till December 31. Under the exemption, notified by the environment ministry on Friday, all such proposals will be appraised for speedy green clearances by putting activities relating to ‘active pharmaceutical ingredients’ (API) under ‘B2’ category projects.

Since projects under ‘B2’ category do not require environment impact assessment (EIA) and public hearings, drug manufacturers can get speedy green clearance. The flexibility is believed will help domestic drug manufacturers self-reliant in the manufacture of APIs which are used as raw materials for producing medicines.

“All proposals for projects or activities in respect of API, received from 16th July, 2021 to 31st December, 2021, shall be appraised as Category ‘B2’ projects,” said the ministry’s notification under the Environment (Protection) Act, 1986.

It, at the same time, clarified that all projects/activities after December 31 would be considered as per the provisions in force at that time.

The ministry in its notification justified the liberal approach in granting green clearance. It said, “The central government deems it necessary to provide another window (of exemption) in view of the second wave of Covid-19 pandemic and continued requirement of expeditious drug manufacturing.”

It noted the ministry had received requests for extension of the time period beyond the earlier one which expired on March 30 as “there is a continued requirement to expedite drug manufacturing”.

Rules notified under the 1986 Act classify projects into three categories – category ‘A’ which needs to be appraised by the ministry, category ‘B’ where states need to give clearance and category ‘B2’ which exempts projects from EIA and public hearing.

Though the ministry had earlier issued notification twice while granting the exemption to drug manufacturers, there was no such specific order beyond March 30.

  • Related Posts

    WHO launches new primary health care course to strengthen health systems globally

    Health is a human right – yet not everyone can access the health services they need, when and where they need them, without financial hardship. Primary health care (PHC) provides…

    Ayurveda needs stronger evidence, safety monitoring for market adoption, says CCRAS

    Bengaluru: The Central Council for Research in Ayurvedic Sciences (CCRAS) has called for stronger scientific evidence, safety monitoring and translation of research into market-ready technologies to improve the credibility and…

    Leave a Reply

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

    You Missed

    WHO launches new primary health care course to strengthen health systems globally

    WHO launches new primary health care course to strengthen health systems globally

    Ayurveda needs stronger evidence, safety monitoring for market adoption, says CCRAS

    Ayurveda needs stronger evidence, safety monitoring for market adoption, says CCRAS

    Yashoda Medicity Successfully Performs High-Risk Kidney Transplant in 28-Year- Old Woman

    Yashoda Medicity Successfully Performs High-Risk Kidney Transplant in 28-Year- Old Woman

    Avacta delivers two clinical stage peptide-drug conjugates to target delivery of toxic payloads into the tumour microenvironment

    Avacta delivers two clinical stage peptide-drug conjugates to target delivery of toxic payloads into the tumour microenvironment

    US FDA approves first gene therapy for paediatric patients with Sanfilippo syndrome type A

    US FDA approves first gene therapy for paediatric patients with Sanfilippo syndrome type A

    Technology and accessibility are key to growth of advanced treatment of heart diseases, says expert

    Technology and accessibility are key to growth of advanced treatment of heart diseases, says expert