HDA Statement on FDA Authorization of Johnson & Johnson COVID-19 Vaccine
ARLINGTON, Va., February 27, 2021 — HDA President and CEO Chester “Chip” Davis, Jr., released a statement regarding the U.S. Food and Drug Administration’s (FDA) granting of an Emergency Use Authorization (EUA) for the Johnson & Johnson (Janssen Biotech) COVID-19 vaccine candidate:
“FDA’s authorization of a third COVID-19 vaccine candidate — a one-dose formulation — delivers additional hope that we will be able to provide more Americans greater access to vaccines while slowing the rate of infection. HDA appreciates the hard work of our manufacturer trading partners and the FDA in providing another option that strengthens the country’s fight against this virus.
Background Information
- HDA Guiding Principles for COVID-19 Vaccine Distribution
- HDA Statement on COVID-19 Vaccine Distribution and Role of Distribution Industry
About the Healthcare Distribution Alliance
The Healthcare Distribution Alliance (HDA) represents primary pharmaceutical distributors — the vital link between the nation’s pharmaceutical manufacturers and pharmacies, hospitals, long-term care facilities, clinics and others nationwide. Since 1876, HDA has helped members navigate regulations and innovations to get the right medicines to the right patients at the right time, safely and efficiently. The HDA Research Foundation, HDA’s non-profit charitable foundation, serves the healthcare industry by providing research and education focused on priority healthcare supply chain issues.
NOTE: This press release was submitted to Urban Milwaukee and was not written by an Urban Milwaukee writer. While it is believed to be reliable, Urban Milwaukee does not guarantee its accuracy or completeness.
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