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Judul          : BPOM Aims to Start Indigenous Vaccine Production by 2022 Second Half

               Nama Media : tempo.co

               Tanggal        : 30 Desember 2021

               Halaman/URL:https://en.tempo.co/read/1544671/bpom-aims-to-start-indigenous-
                               vaccine-production-by-2022-second-half

               Tipe Media      : Online

                                                         TEMPO.CO, Jakarta - Head  of  the  National

                                                         Agency  of  Drug  and  Food  Control  (BPOM),
                                                         Penny  Lukito,  has  said  that  the  agency  is
                                                         aiming  to  start  production  of  the  Red  and
                                                         White vaccine in the second half of 2022.

                                                         “The  Red  and  White  vaccine  (developed)
               from the collaboration between Airlangga University and PT. Biotis is currently in
               production for clinical trials. The clinical trials will commence soon. We are targeting
               the  production  to  start  in the  second  half  of  2022,” she  informed  during  a media
               briefing on Wednesday.

               Meanwhile,  the  production  of  the  vaccine  developed  by  Bio  Farma  and  Baylor
               College Medicine is also targeted to start in the second half of 2022, she added.

               She said the agency will soon issue emergency-use authorization (EUA) for booster
               vaccines.

               "Currently, vaccines that are in the registration process to be used as boosters are

               Pfizer, AstraZeneca, Zlifivax, and CoronaVac or Biofarma’s COVID-19 vaccine, while
               the Sinopharm vaccine is still in the pre-registration process," she added.

               Meanwhile, BPOM has so far permitted Favipiravir, Remdesivir, and Regdanvimab
               for emergency use.

               "After the issuance of the emergency-use authorization, we carry out post-market
               surveillance to ensure the drugs are being distributed properly, as well as (conduct)
               pharmacovigilance  of  adverse  events  following  immunization  or  AEFIs,"  she
               explained.


               The Indonesian government launched a nationwide vaccination program on January
               13, 2021, in a bid to boost immunity against COVID-19.
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