Govt issues regulatory pathways for foreign produced Covid-19 vaccines

This is aimed at facilitating quicker access to such foreign vaccines by India to encourage imports including bulk drug material, optimal utilization of domestic fill and finish capacity

New Delhi: In a radical reform measure, the Centre on Thursday issued Regulatory Pathway in India for Covid-19 vaccines approved for restricted use in the US, the UK, Japan or which are listed in the WHO's emergency use listing.

After comprehensive deliberation, the National Expert Group on Vaccine Administration for Covid-19 (NEGVAC), chaired by Niti Aayog member (Health) Dr VK Paul, issued the Regulatory Pathway for Covid-19 vaccines approval for "restricted use by US FDA, EMA, UK MHRA, PMDA Japan or which are listed in WHO Emergency Use Listing (EUL)".

The decision has been taken amid an unprecedented surge in Covid cases in the country with over 2 lakh people were infected on a single day, claiming 1,73,123 lives so far.

The government on April 13, had approved a significant streamlining and fast tracking of regulatory system for these foreign produced vaccines.

This decision aimed at facilitating quicker access to such foreign vaccines by India to encourage imports including bulk drug material, optimal utilization of domestic fill and finish capacity, which will in turn provide a fillip to vaccine manufacturing capacity and total vaccine availability within the country.

Considering the step, the Central Drugs Standards Control Organization (CDSCO) headed by Drugs Controller General of India (DCGI) on Thursday explained the pathway that include preparation for detailed guidelines for approval of foreign approved Covid vaccines based on NEGVAC recommendations.

"These guidelines have since been prepared and posted by CDSCO on its website. The CDSCO will take steps to widely disseminate these guidelines to the concerned stakeholders," the Ministry said.

Applicants for grant of approval for Restricted Use in Emergency situation may be submitted to CDSCO, said the Ministry, adding application can be made by the foreign manufacturer through its Indian subsidiary or through its authorized agent in India (in case it does not have an Indian subsidiary). The CDSCO will process such applications for restricted use in emergency situation and DCGI will consider and take a decision within three working days from date of submission of complete application by the applicant.

The DCGI will issue permission for restricted use in emergency situation with conditions like Vaccine shall be used as per the guidelines prescribed under national Covid-19 vaccination programme.

"First 100 beneficiaries of such vaccines shall be assessed for seven days for safety outcomes before it is rolled out for further vaccination program. Applicant shall initiate conduct of post approval bridging clinical trials within 30 days of such approval."