McKesson is a centralized distribution partner for the US government's COVID vaccine distribution effort.
The Janssen vaccine received Emergency Use Authorization from the US Food and Drug Administration on Feb. 27 and is the first one-shot COVID-19 vaccine to be authorized for use in the United States.
McKesson was selected by the US government in August 2020 to operate as the centralized distributor for frozen and refrigerated COVID-19 vaccines and ancillary supply kits needed to administer them.
In December 2020, McKesson began distributing the ancillary supply kits for Pfizer BioNTech's COVID-19 vaccine.
Later that month, the company began distributing Moderna's COVID-19 vaccine and ancillary supply kits.
McKesson has established four dedicated distribution centers which will be specifically used to distribute the Johnson and Johnson COVID-19 vaccine and future refrigerated vaccines.
The US government makes all program administration decisions, including where, when and how many vaccine doses McKesson will distribute.
McKesson is a healthcare supply chain management solutions, retail pharmacy, community oncology and specialty care, and healthcare information solutions company.
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Lupin launches Dasatinib tablets in US market
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA
FDA approves Tenpoint Therapeutics' YUVEZZI as first dual-agent eye drop for presbyopia
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
WuXi Biologics collaborates with Sinorda Biomedicine for antibody development
Biogen's litifilimab receives FDA Breakthrough Therapy Designation for CLE
Glaukos receives FDA approval for repeat administration of iDose TR
Guerbet's contrast agent Elucirem approved by European Commission in children from birth
Spine Innovation's LOGIC Titanium Implant System receives US FDA 510(k) market approval