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BioWorld - Friday, March 13, 2026
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Regulatory front

MHRA: Trial supply chains need to prepare for Brexit changes

Dec. 14, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: Health Canada to extend COVID-19 flexibilities; USTR seeking input on nations with poor IP protections.
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Regulatory actions for Dec. 14, 2020

Dec. 14, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbvie, Acceleron, Amag, Ascletis, Antengene, Astrazeneca, Avelas, Biontech, Codagenix, Daiichi Sankyo, EMD, Gamida, Gannex, Graphite, Legend, Merck KGaA, Mindmed, Open Orphan, Pfizer, Sobi.
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Leqvio approved in Europe for the treatment of hypercholesterolemia or mixed dyslipidemia

Dec. 14, 2020
Product image

Sounds good! Advanced Bionics receives FDA approval of Marvel cochlear implant platform

Dec. 11, 2020
By Annette Boyle
Advanced Bionics LLC heard good news from the U.S. FDA, which granted approval for the company’s Marvel cochlear implant (CI) platform and the first-ever sound processor designed specifically for children. The development brings the Marvel platform, initially created for hearing aids produced by Advanced Bionics' sister company, Phonak AG, to the sound processor for CIs for the first time.
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Regulatory actions for Dec. 11, 2020

Dec. 11, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Applied Biocode.
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Regulatory front

FDA posts three guidances under safety and performance program

Dec. 11, 2020
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: FDA delays comment period for electromagnetic compatibility draft; CMS, ONC post info sharing, prior authorization rule; Van Hollen debuts diagnostic accuracy bill; CDC updates POC testing guidelines; GAO: Specimen biopsy handling errors relatively low.
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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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Pfizer, Biontech win FDA’s first COVID-19 vaccine authorization

Dec. 11, 2020
By Michael Fitzhugh
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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