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BioWorld - Monday, December 22, 2025
Home » Topics » Regulatory, BioWorld

Regulatory, BioWorld
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EMA’s CHMP delivers eight positive opinions in December, 61 for 2020

Dec. 11, 2020
By Cormac Sheridan
DUBLIN – The European Medicines Agency’s human medicines committee, the CHMP, all but closed out the year by issuing positive opinions on eight marketing authorization applications during its December meeting. Its work for 2020 is not quite yet done, however. It has scheduled an extraordinary meeting for Dec. 29 to review an application from Pfizer Inc. and Biontech AG for their mRNA COVID-19 vaccine BNT162b2.
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Regulatory actions for Dec. 11, 2020

Dec. 11, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Arix, Biogen, Bristol Myers Squibb, Daiichi Sankyo, Dynavax Technologies, Excellthera, Gilead Sciences, Janssen, Lexicon, Merck, Passage, Sanofi, Seagen, Soleno, V2act, Viiv Healthcare, Xeris.
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Vaccine administration

Vaccine EUA not a total slam dunk with adcom

Dec. 10, 2020
By Mari Serebrov
The FDA’s vaccine advisory committee voted 17-4 with one abstention Dec. 10 to recommend an emergency use authorization (EUA) for the Pfizer Inc./Biontech SE mRNA vaccine BNT-162b2 to prevent COVID-19 in individuals 16 and older.
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Regulatory actions for Dec. 10, 2020

Dec. 10, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Atox, Biogen, Diamedica, Editas, Eisai, Entera, Hoth, Lantheus, Neoleukin, Oblato, Scynexis, SOBI, Ultragenyx, X4.
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Regulatory front

Canada follows the U.K. in approving COVID-19 vaccine

Dec. 9, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: Sacklers threatened with House subpoena; DEA proposes de-scheduling Alkermes drug; Marburg MCMs protected under PREP; OPDP: Don’t make risks a P.S.; U.S. Senators sound off on E&M offsets.
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Regulatory actions for Dec. 9, 2020

Dec. 9, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: 9 Meters, Albireo, Amryt, Bebig, Beigene, Citius, Chugai, Lipocine, Pfizer, Rafarma, Sinovac, Sorrento, Tricida, Tvax, United, Valeo.
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Regulatory front

What’s not in a drug name is important

Dec. 8, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: USPTO finalizes SAS rule.
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Regulatory actions for Dec. 8, 2020

Dec. 8, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Amgen, Beigene, Cerecor, Cyxone, Henlius, ITM, Ix, Takeda, Turning Point.
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Pills and bottle

After years of effort, Japan slashes drug lag

Dec. 7, 2020
By Alfred Romann
TOKYO – Steadily over a decade and a half, Japan’s drugs and devices regulator has all but eliminated a huge drug lag that put the second largest drug market in the world well behind most others in terms of the time it took for approvals and patient access to innovative drugs.
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Coronavac shipment

Brazil’s Anvisa issues emergency pathway for COVID-19 vaccines, though some firms seek other routes

Dec. 7, 2020
By Sergio Held
Brazilian health care regulator Anvisa has issued guidelines for SARS-CoV-2 vaccine manufacturers to receive emergency marketing approvals in the Latin American giant. Brazil is the largest market in the region and several COVID-19 vaccine makers are both doing trials there and hoping for quick approvals.
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