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

BioWorld, Regulatory
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2021 China Pharmaceutical Innovation 100 Summit

Regulators need to up their game to support drugmakers’ global drug development, experts urge

April 13, 2021
By Elise Mak
Speaking during the 2021 China Pharmaceutical Innovation 100 Summit, industry insiders called for more regulatory talent and even an organizational revamp to clear innovative products faster and support the global development strategies of Chinese drugmakers.
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2021 China Pharmaceutical Innovation 100 Summit

China launches policies to encourage innovation, but pricing and payment remain pain points

April 13, 2021
By Elise Mak
SHANGHAI – China’s regulatory environment has evolved to encourage drug innovation, but despite remarkable progress, mounting pricing pressure from the government and a weak insurance sector remain as barriers.
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FDA icons

Adcom to explore first islet cell therapy for diabetes relief

April 13, 2021
By Mari Serebrov
The FDA’s Cellular, Tissue and Gene Therapies Advisory Committee will be venturing into new territory April 15 in which it not only has to consider whether the benefit of Celltrans Inc.’s donislecel is clinically meaningful, but it also will have to define the indication.
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Regulatory actions for April 13, 2021

April 13, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Akouos, Avenue, Axcella Health, Celularity, Janssen, Kibow, Lintonpharm, Neuraptive, Novartis, RDIF, Vtv.
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Syringe with Johnson & Johnson logo

Rare clotting cases prompt FDA, CDC to pause rollout of J&J COVID-19 vaccine

April 13, 2021
By Cormac Sheridan
The FDA and the CDC have jointly recommended a temporary pause in the further rollout of Johnson & Johnson Co.’s COVID-19 vaccine while they investigate six rare clotting cases in adults ages 18 to 48.
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Cavazzoni no longer acting

April 12, 2021
By Mari Serebrov
The “acting” has been dropped from Patrizia Cavazzoni’s title as director of the U.S. FDA’s Center for Drug Evaluation and Research (CDER).
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India battles remdesivir shortages

April 12, 2021
By Mari Serebrov
With shortages of the COVID-19 drug, remdesivir, being reported in several states in India, the country’s Central Drugs Standard Control Organization is calling on state regulators to “immediately initiate remedial action to ensure supply of remdesivir injection to public and private hospitals.”
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MACPAC tackles 'accelerated' prices

April 12, 2021
By Mari Serebrov
If the U.S. Congress is receptive to recommendations approved by the Medicaid and CHIP Payment and Access Commission (MACPAC) April 9, the FDA's accelerated approval path for innovative new drugs could lose a bit of its appeal. And sponsors using that path may speed the pace of seeking full approval.
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Astrazeneca vaccine risk prompts Australian government to recommend Pfizer COVID-19 vaccine for under 50

April 12, 2021
By Tamra Sami
PERTH, Australia – The Australian government is recommending that Australians under 50 take the Pfizer Inc. COVID-19 vaccine due to the risk of rare blood clots associated with Astrazeneca plc’s COVID-19 vaccine (ChAdOx1-S). The move jeopardizes Australia’s vaccine rollout as it had planned for the majority of Australians to receive the Astrazeneca vaccine, which is being locally manufactured by CSL Ltd.
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Regulatory actions for April 12, 2021

April 12, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Adamis, Airway, Akari, Biontech, Generex, Genmab, Jazz, Junshi, Nugenerex, Pfizer, Resverlogix, Scolex, Seagen, Sorrento.
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