$BioNTech SE(BNTX)$https://www.nytimes.com/2021/08/11/us/politics/third-vaccine-dose-approval.htmlF.D.A. to Authorize Third Vaccine Dose for People With Weak Immune Systems
$Novavax(NVAX)$The interest in Novavax increases as countries one by one, come on board to book their doses. https://www.reuters.com/world/europe/denmark-buy-novavax-vaccines-part-eu-deal-2021-08-11/
$Novavax(NVAX)$WHO webinar starts August 13 13:00 CET:WHO consultation on COVID-19 vaccines research – 13 August 202113 August 2021 13:00 – 18:00 CETIn continuation to the scientific discussions on COVID-19 vaccines research, WHO R&D Blueprint is organizing a consultation on the state of the art and best research methods to evaluate existing, modified and new COVID-19 vaccines.The objectives of this forthcoming consultation will be to review the available evidence on the efficacy and effectiveness of vaccines being deployed in terms of:Emerging variants effect on protection levels Duration of protectionSafety of booster vaccinesResearch to evaluate various delivery strategieshttps://www.who.int/news-room/events/detail/2021/08/13/default-calendar/
$Novavax(NVAX)$GAITHERSBURG, Md., Sept. 23, 2021 /PRNewswire/ -- Novavax, Inc. (Nasdaq: NVAX), a biotechnology company dedicated to developing and commercializing next-generation vaccines for serious infectious diseases, with its partner, Serum Institute of India Pvt. Ltd. (SII), today announced a regulatory submission to the World Health Organization (WHO) for emergency use listing (EUL) of Novavax' recombinant nanoparticle protein-based COVID-19 vaccine candidate with Matrix-MTM adjuvant. The submission to WHO is based on the companies' previous regulatory submission to the Drugs Controller General of India (DCGI)."Today's submission of our protein-based COVID-19 vaccine to WHO for emergency use listing is a significant step on the path to accelera