The
resumption comes after J&J last week slashed its 2021 production
target of its single-dose vaccine to between 500 million and 600
million doses from its original goal to produce a billion shots.
The resumption follows additional reviews and collaboration with
the FDA and manufacturing partners, Emergent Chief Executive
Officer Robert Kramer said.
The FDA has so far approved five batches from the Emergent
facility since production there was paused, and J&J is working
to clear additional doses for use, the drugmaker said last week.
U.S. health regulators in April halted operations at the
Baltimore plant following a discovery that ingredients from
AstraZeneca's COVID-19 vaccine, also being produced there at
that time, contaminated a batch of J&J's vaccines.
An FDA inspection also turned up a long list of sanitary
problems and bad manufacturing practices.
J&J's vaccine, considered more convenient for use, storage and
shipping to remote areas, has seen a relatively slow uptake in
Europe and the United States due to safety concerns and the
production issues.
Johnson & Johnson and the FDA did not immediately respond to
Reuters requests for comment.
The Wall Street Journal, which first reported the news, cited a
letter from the FDA saying the agency had no objections with the
plant resuming manufacturing.
The facility could make as many as 120 million doses a month at
full capacity, but the finished doses might not be available
until this fall, the Journal reported, citing a source.
(Reporting by Aishwarya Nair, Maria Ponnezhath and Manojna
Maddipatla in Bengaluru; Editing by Subhranshu Sahu,
Ramakrishnan M. and Shounak Dasgupta)
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