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BioWorld - Friday, June 19, 2026
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Home » Topics » BioWorld, Regulatory

BioWorld, Regulatory
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COVID-19 vaccine and syringe with flag of China

China widens COVID-19 booster choices

Feb. 22, 2022
By Mari Serebrov
China is the latest country mixing things up when it comes to COVID-19 boosters. Since boosters were implemented in China in October, adults have been given a third dose of their primary vaccine regimen, which has consisted of one of three inactivated vaccines produced by Sinopharm Group Co. Ltd. and Sinovac Biotech Ltd.
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Regulatory actions for Feb. 22, 2022

Feb. 22, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Agios, Biomarin, Dizal, Novavax, Ose, Transthera, UCB, Veloxis.
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EMA icons

EMA: Increase in NCEs approved amid overall drop for 2021 and continued COVID-19 pressure

Feb. 18, 2022
By Nuala Moran
LONDON – Two years into the pandemic and the number of new drugs approved by the EMA fell from 97 approvals in 2020 to 92 in 2021. But both years are still well up on pre-COVID-19 times in 2019 when 66 products got the nod, according to the EMA’s annual human medicines report.
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Red blood cells

Agios’ pivot from oncology leads to an FDA approval in rare disease

Feb. 18, 2022
By Lee Landenberger
The FDA’s approval of Agios Therapeutics Inc.’s Pyrukynd (mitapivat) for treating hemolytic anemia marks a turnaround from nearly a year ago. That’s when Agios sold its commercial, clinical and research-stage oncology portfolio to privately held Servier Pharmaceuticals LLC to concentrate on rare diseases.
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US FDA targets remdesivir with product-specific guidance

Feb. 18, 2022
By Mari Serebrov
As part of its ongoing effort to speed drug pricing competition in the U.S. through the development of generics, the FDA is releasing another batch of draft and revised draft product-specific guidances on the design of bioequivalence studies to support abbreviated new drug applications. Among the 30 new draft guidances is one specific to remdesivir, which was approved in October 2020 as a COVID-19 treatment.
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Reichstag, German parliament building in Berlin

European Besremi legal tussle continues

Feb. 18, 2022
By Mari Serebrov
In the latest chapter in an ongoing contract dispute between AOP Orphan Pharmaceuticals GmbH and Pharmaessentia Corp., the German Federal Court of Justice this week set aside the €143 million (US$162.8 million) in damages awarded to AOP, citing procedural flaws in quantifying the product supply and damages.
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Regulatory actions for Feb. 18, 2022

Feb. 18, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Amylyx, AN2, Astrazeneca, Beigene, BMS, Cstone, Epygenix, Immune-Onc, Kato, Lupin, Moderna, Poxel, Sanofi, Valbiotis, Zai Lab.
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Flag of India

India’s health care industries receive mixed messages from authorities

Feb. 17, 2022
By David Ho
India’s health care industry stakeholders have been left scratching their head as authorities, who have championed self-reliance and increased supplies, provided mixed signals in recent notices.
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US flag, Department of Health and Human Services flags

Court: US HHS violation letters violative

Feb. 17, 2022
By Mari Serebrov
Drug companies won another round in their battle with the U.S. Department of Health and Human Services (HHS) over how many contract pharmacies must be given the steep discounts dictated under the 340B drug pricing program aimed at helping public clinics and hospitals provide charity care.
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Francis Collins, director, U.S. NIH

Collins temporarily assigned new scientific role in US government

Feb. 17, 2022
By Mari Serebrov
As the Biden administration continues to play musical chairs with key U.S. federal health leadership positions, its latest move is naming Francis Collins to serve as science adviser to the president and co-chair of the President’s Council of Advisers on Science and Technology.
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