Unlike the Covid-19 drugs, such as remdesivir and favipiravir, which were allowed only a three-month shelf life after they got restricted emergency-use authorisation from the Indian regulator, vaccines now may be allowed a longer shelf life, revealed people in the know.
Vaccine makers have been conducting early animal testing since May/June. They have the stability data for these investigational products, said a source. "The vaccines will be allowed a shelf life of six months or more since the makers have the data for this period," said a pharmaceutical executive.
The stability of a drug or vaccine refers to the extent to which a drug substance retains the same properties and characteristics it possessed at the time of its manufacture. This is used to determine the shelf life or expiration dates of drugs.
A longer shelf life is critical, given many makers have started manufacturing vaccines and stockpiling them, so as to make them available in the market immediately after approval.
Around June, repurposed drugs like remdesivir (originally developed for ebola by Gilead Sciences, Inc.) and favipiravir (for influenza) were given restricted emergency-use authorisation by the Drugs Controller General of India. At that time, these drugs were allowed a shelf life of just three months.
Vaccine makers have been conducting early animal testing since May/June. They have the stability data for these investigational products, said a source. "The vaccines will be allowed a shelf life of six months or more since the makers have the data for this period," said a pharmaceutical executive.
The stability of a drug or vaccine refers to the extent to which a drug substance retains the same properties and characteristics it possessed at the time of its manufacture. This is used to determine the shelf life or expiration dates of drugs.
A longer shelf life is critical, given many makers have started manufacturing vaccines and stockpiling them, so as to make them available in the market immediately after approval.
Around June, repurposed drugs like remdesivir (originally developed for ebola by Gilead Sciences, Inc.) and favipiravir (for influenza) were given restricted emergency-use authorisation by the Drugs Controller General of India. At that time, these drugs were allowed a shelf life of just three months.

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