Summary:
New Delhi, Sep 17 (PTI) There will not be a third wave of Covid of the size and consequence the country witnessed during the second wave unless there is a new variant of coronavirus, top vaccinologist Gagandeep Kang said Friday.She stressed the need to develop better vaccines that can deal with new variants, and strengthening of the regulatory mechanisms."Unless there is a new variant there will not be a third wave of the size and consequences that we saw in the second wave.
What we will see is local flare-ups where there are unprotected populations and where the virus has not been before," Kang said.The second wave of coronavirus in the country between March and May killed thousands and infected lakhs, overwhelming the health infrastructure.
"Are we done with COVID? No we are not.
Are we going to be done with COVID? Not anytime in the near future," she added.Kang, a professor with Christian Medical College, Vellore, was speaking virtually at the CII Lifesciences Conclave.Last month, Manindra Agrawal, a scientist with IIT-Kanpur who is in the three-member team of experts tasked to project the surge in cases, had said the country may see a third wave peaking between October-November if a more virulent mutant of coronavirus emerges by September.Kang said the Indian vaccine industry has been “absolutely phenomenal” in dealing with the pandemic, but it still has a long way to go."I can"t say the same thing (about the regulatory system) as people know about our regulatory systems.
But it is something we should use as a lesson for the future because we really really need informed, strong regulators that work with industries to show what is required," she said.Kang also stressed the need for a translational research ecosystem of clinical researchers that are willing to take risk, and are supported by the government and academia.She said new technologies carry risks and there is a need for a regulatory system that is prepared for clinical risks."We need the academic medical environments that work with the industry to make sure that we can safely test these interventions in people.
We do not have this at this time so strengthening regulation is key." She said surveillance diagnostics is still dependent very heavily on imports.