We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
  • SKIP TO CONTENT
  • SKIP NAVIGATION
  • Drug Products
    • Books
    • FDAnews Books Library
    • Events
    • Form 483s Database
    • Subscription Newsletters
    • Free Newsletters
    • Webinar Training Pass
    • eCFR and Guidances
  • Device Products
    • Books
    • FDAnews Books Library
    • Events
    • Form 483s Database
    • Subscription Newsletters
    • Free Newsletters
    • Webinar Training Pass
    • eCFR and Guidances
  • Clinical Products
  • Advertising
  • White Papers
  • Contact Us
  • About Us
  • COVID-19
  • Sign In
  • Create Account
  • Sign Out
  • My Account
Home » U.S. Vaccinations to Start Today Following FDA’s Emergency Clearance for Pfizer/BioNTech Vaccine

U.S. Vaccinations to Start Today Following FDA’s Emergency Clearance for Pfizer/BioNTech Vaccine

December 14, 2020

The first U.S. COVID-19 vaccinations are to be given today using Pfizer/BioNTech’s vaccine, following the announcement late Friday that the FDA had granted the first emergency clearance for a coronavirus vaccine, a pivotal and unprecedented moment in the battle against the pandemic.

Pfizer is employing its own strategy for distribution due to its experience in cold-chain shipping and existing infrastructure. The initial roll-out of its vaccine consists of 2.9 million doses, with the other 2.9 million doses — the second round of shots — to be shipped later, HHS Secretary Alex Azar said Sunday.

Pfizer’s vaccine needs to be shipped with dry ice at the extremely cold temperature of -94 Fahrenheit (F), a requirement that presents serious logistical considerations. The drugmaker is delivering special packaging and storage technology to vaccination sites that will keep doses safe for 10 days (DID, Nov. 4). Pfizer will deliver the vaccine doses to state health authorities, who will distribute it to frontline healthcare workers and the elderly (DID, Dec. 9).

Gen. Gustave Perna, chief operating officer of Operation Warp Speed (OWS), said over the weekend that the government expects nearly 150 vaccination sites to receive the first vials of the two-dose vaccine today, with more to get supplies as the week goes on. By mid-week the initial vaccine deliveries, which total 2.9 million doses, are due to be completed.

“When the decision occurred [on Friday], we immediately went into action,” Perna said. “We expect 145 sites across all the states to receive vaccine on Monday, another 425 sites on Tuesday, and the final 66 sites on Wednesday, which will complete the initial delivery of the Pfizer orders for vaccine,” he said.

Deliveries of BNT162b2 — from a Pfizer plant in Kalamazoo, Mich. — started over the weekend, said Nancy Messonnier, director of the Center for Disease Control and Prevention (CDC)’s Center for Immunization and Respiratory Diseases, and CDC Director Robert Redfield on Sunday approved the recommendation of the CDC’s immunization practices panel in support of the vaccine. The panel voted Saturday in favor of the vaccine.

President Trump had pressured the FDA and Commissioner Stephen Hahn to get the Emergency Use Authorization (EUA) for the Pfizer vaccine signed by Friday night, calling the agency “money drenched but heavily bureaucratic” and “still a big, old, slow turtle.” White House Chief of Staff Mark Meadows reportedly warned Hahn he would have to resign if the EUA wasn’t done Friday, an allegation Hahn disputes, though the agency did end up meeting the administration’s timeline.

“There was a desire for us to move as quickly as possible,” Hahn said. “We have. We had to get this right and I believe we did.”

The EUA for the two-dose Pfizer vaccine came a day after the agency’s vaccine advisory committee voted 17-4, with one abstaining vote, in favor of awarding an EUA for use of the highly effective vaccine in patients ages 16 and above. At least two ‘no’ voters had expressed hesitancy toward the EUA due to a lack of data for 16- and 17-year-old patients (DID, Dec. 11).

Moncef Slaoui, OWS’ chief adviser, said Sunday that the federal government plans to have about 40 million Pfizer and Moderna vaccine doses distributed in the U.S. by the end of the year. It should have approximately 50 million to 80 million doses of vaccines distributed in January and plans to distribute the same amount in February, he said.

“We hope to have immunized 100 million people, which would be the long-term care facility people, the elderly people with comorbidities, the first-line workers, the healthcare workers … we will have immunized about 100 million people by the first quarter of 2021,” Slaoui said.

Moderna on Friday announced that the U.S. has exercised its option to order 100 million additional vaccine doses, bringing its total amount ordered to 200 million shots.

The vaccine advisory committee meets again on Dec. 17 to discuss an EUA for Moderna’s promising two-dose COVID vaccine, and a recommendation in favor of an EUA is expected. — James Miessler

COVID-19

Upcoming Events

  • 21Jan

    Virtual MDSAP Audits in the Era of COVID-19: What to Know and Do to Pass Virtual Audits

  • 26Jan

    Reducing Complexity in Starting Clinical Trials – More Patients, Faster Startup

  • 27Jan

    Medical Device Clinical Trials in China: Latest Regulatory Developments

  • 27Jan

    FDA’s Response to COVID-19: Fundamentals of Obtaining Emergency Use Authorizations

  • 09Feb

    Maintaining Your Risk-Based Cleaning and Disinfectant Programs: Best Practices During COVID-19

  • 10Feb

    FDA Under the Biden Administration: What’s to Come and What It Will Mean

Featured Products

  • Biological Risk Evaluation and Management for Medical Devices

  • GMP Inspection Preparation Checklist: A Tool for Internal Auditing

Featured Stories

  • COVID-19  Clinical Trial

    Synairgen Initiates Dosing in Late-Stage Trial of Inhaled COVID-19 Therapy

  • Verona Pharma logo

    Verona Pharma Ends Enrollment in Inhaler-Administered COVID-19 Drug Pilot

  • Purple_Approved_Stamp.gif

    Seno Medical Gets Premarket Approval for Breast Cancer Diagnostic

  • Triple Vaccine, needles

    Moderna to Start New Trial Adding Third Shot of COVID-19 Vaccine

The Revised ICH E8: A Guide to New Clinical Trial Requirements

Learn More
  • Drug Products
    • Quality
    • Regulatory Affairs
    • GMPs
    • Inspections and Audits
    • Postmarket Safety
    • Submissions and Approvals
    • Research and Development
    • Commercial Operations
  • Device Products
    • Quality
    • Regulatory Affairs
    • QSR
    • Inspections and Audits
    • Postmarket Safety
    • Submissions and Approvals
    • Research and Development
    • Commercial Operations
  • Clinical Products
    • Trial Design
    • Data Integrity
    • GCP
    • Inspections and Audits
    • Transparency
  • Privacy Policy
  • Do Not Sell My Personal Information
Footer Logo

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

Phone 703.538.7600 – Fax 703.538.7676 – Toll free 888.838.5578

Copyright © 2021. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing