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5 Slides: Bending the Rx cost curve - State of Reform

5 Slides: Bending the Rx cost curve - State of Reform
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Moderna gets emergency use authorisation for its Covid vaccine in US

Moderna gets emergency use authorisation for its Covid vaccine in US
Second company after Pfizer to receive nod
Moderna has become the second company to get emergency use authorisation for its anti-coronavirus vaccine from the US Food and Drug Administration (FDA), a week after the one developed by Pfizer received similar approval.
According to an official statement, the FDA has determined that the Moderna Covid-19 vaccine has met the statutory criteria for issuance of an emergency use authorisation (EUA).
Congratulations, the Moderna vaccine is now available! President Donald Trump tweeted soon after.
The FDA based its recommendation on the totality of scientific evidence shared by Moderna, including a data analysis from the pivotal phase three clinical study announced on November 30. The primary efficacy analysis conducted on 196 cases indicated a vaccine efficac ....

United States , Alex Azar , Michael Burgess , Stephenm Hahn , Moderna Covid , Donald Trump , Mike Pence , Centers For Disease , Department Of Defense , Human Services , National Institutes Of Health , Drug Administration , House Rules Committee , Advisory Committee On Immunization Practices , Commerce Subcommittee On Health , Republican Leader Of The House Energy , Department Of Health , President Mike Pence , Secretary Alex Azar , National Institutes , Biologics License Application , Chief Executive Officer , Disease Control , Advisory Committee , Immunization Practices , Operation Warp Speed ,

After Pfizer, US authorizes Moderna COVID-19 vaccine for emergency use

US added a second COVID-19 vaccine to its arsenal
Food and Drug Administration authorized an emergency rollout of the vaccine developed by Moderna Inc. And the National Institutes of Health.
The move marks the world s first authorization for Moderna s shots.
WASHINGTON: Moderna has become the second company to get emergency use authorisation for its anti-coronavirus vaccine from the US Food and Drug Administration (FDA), a week after the one developed by Pfizer received a similar approval.
According to an official statement, the FDA has determined that the Moderna COVID-19 vaccine has met the statutory criteria for issuance of an emergency use authorisation (EUA). ....

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Moderna Gets Emergency Use Authorisation For Its COVID 19 Vaccine In US

BW Businessworld
Moderna Gets Emergency Use Authorisation For Its COVID-19 Vaccine In US
According to an official statement, the FDA has determined that the Moderna COVID-19 vaccine has met the statutory criteria for issuance of an emergency use authorisation (EUA).
Photo Credit :
Moderna has become the second company to get emergency use authorisation for its anti-coronavirus vaccine from the US Food and Drug Administration (FDA), a week after the one developed by Pfizer received a similar approval.
According to an official statement, the FDA has determined that the Moderna COVID-19 vaccine has met the statutory criteria for issuance of an emergency use authorisation (EUA). ....

United States , Alex Azar , Michael Burgess , Stephenm Hahn , Donald Trump , Mike Pence , Centers For Disease , Human Services , Department Of Defense , National Institutes Of Health , Drug Administration , House Rules Committee , Advisory Committee On Immunization Practices , Commerce Subcommittee On Health , Republican Leader Of The House Energy , Department Of Health , President Mike Pence , Secretary Alex Azar , National Institutes , Biologics License Application , Chief Executive Officer , Disease Control , Advisory Committee , Immunization Practices , Operation Warp Speed , Republican Leader ,

Moderna gets emergency use authorisation for its COVID-19 vaccine in US

Moderna gets emergency use authorisation for its COVID-19 vaccine in US
Representative Image
Moderna has become the second company to get emergency use authorisation for its anti-coronavirus vaccine from the US Food and Drug Administration (FDA), a week after the one developed by Pfizer received a similar approval.
According to an official statement, the FDA has determined that the Moderna COVID-19 vaccine has met the statutory criteria for issuance of an emergency use authorisation (EUA).
Congratulations, the Moderna vaccine is now available! President Donald Trump tweeted soon after.
The FDA based its recommendation on the totality of scientific evidence shared by Moderna, including a data analysis from the pivotal phase three clinical study announced on November 30. The primary efficacy analysis conducted on 196 cases indicated a vaccine efficacy rate of 94.1 per cent. ....

United States , Alex Azar , Michael Burgess , Stephenm Hahn , Donald Trump , Mike Pence , Centers For Disease , Human Services , Department Of Defense , National Institutes Of Health , Drug Administration , House Rules Committee , Advisory Committee On Immunization Practices , American National Institutes Of Health , Commerce Subcommittee On Health , Republican Leader Of The House Energy , Department Of Health , President Mike Pence , Secretary Alex Azar , National Institutes , Biologics License Application , Chief Executive Officer , Disease Control , Advisory Committee , Immunization Practices , Operation Warp Speed ,