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The COVID-19 pandemic has led to many changes in how pharmaceutical companies develop vaccines.
More technologies and treatments are emerging for COVID-19—along with new variants.
Partnerships formed during the COVID-19 pandemic have provided a platform for change in assay development and transfers.
December 08, 2020
Pfizer-BioNTech details its case for Emergency Use Authorization for "highly effective" COVID-19 vaccine.
December 04, 2020
A longer-than-expected scale up of raw materials forces Pfizer to cut 2020 vaccine production in half.
December 03, 2020
Janssen announces rolling submissions for its COVID-19 vaccine with Health Canada and EMA.
December 02, 2020
Pharmaceutical laboratories must keep lab data integrity practices in mind in order to properly handle the effects of the COVID-19 pandemic.
After a difficult year, bio/pharma science delivers promising results.
Transparency and open-dialogue are vital to sway the vaccine-hesitant community.
MHRA has granted a temporary authorization for emergency use to Pfizer and BioNTech for the mRNA vaccine against COVID-19.
December 01, 2020
Moderna has filed for authorization for its COVID-19 vaccine candidate, which has shown high efficacy and safety in a Phase III trial.
A holistic approach to validation and quality assurance is essential.
November 24, 2020
FDA granted fast track designation for AB201, a small recombinant protein that is a potent, selective inhibitor of tissue factor, for the potential treatment of COVID-19.