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BioWorld - Sunday, March 1, 2026
Home » Topics » Regulatory, BioWorld

Regulatory, BioWorld
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Regulatory front

Senators eye patent examiner practice for Section 101 problem

March 25, 2021
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for March 24, 2021

March 24, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Akebia, Ascentage, Berg, Enterome, Horizon, RDIF, Reneo.
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Bipartisan agreement: Time to do something about U.S. Rx prices

March 23, 2021
By Mari Serebrov
If the biopharma industry thought its round-the-clock efforts and considerable financial investments in tackling COVID-19 would earn it good will in the U.S. Congress, those hopes were dashed March 23 when both Democrats and Republicans serving on a Senate Health, Education, Labor and Pensions subcommittee reverted to blaming drug companies for much of what’s wrong with the U.S. health care system.
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Australia and coronavirus syringe

Australia’s TGA clears local manufacture of Astrazeneca’s COVID-19 vaccine

March 23, 2021
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Goods Administration (TGA) has approved Australian manufacture of Astrazeneca plc’s COVID-19 vaccine (ChAdOx1-S), which is being manufactured by CSL Ltd.
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Regulatory front

MHRA puts patients in pilot seat

March 23, 2021
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: End of the road for ‘standing’ case; TGA gives labeling guidance; Trial fraud leads to prison sentences.
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Regulatory actions for March 23, 2021

March 23, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Amryt, Cansino, Incyte, Insmed, JCR, Merck, Protagonist, RDIF, Zealand.
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Lengthy joint adcom on tap for Pfizer’s osteoarthritis drug

March 23, 2021
By Mari Serebrov
With the December PDUFA date already blown, Pfizer Inc. is headed into a day-and-a-half FDA advisory committee meeting this week to make the case for 2.5-mg tanezumab, a potential first-in-class treatment in the U.S., partnered with Eli Lilly and Co. Inc., for chronic pain due to moderate to severe osteoarthritis.
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Adult checking child blood glucose level

Three of a kind in glucagon game as FDA turns over Zealand’s card

March 23, 2021
By Randy Osborne
“We’re launching at the right time,” said Frank Sanders, president of Zealand Pharma A/S’s business in the U.S., in the wake of clearance granted by the FDA for the Copenhagen, Denmark-based firm’s glucagon analogue Zegalogue (dasiglucagon) in severe hypoglycemia.
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Regulatory front

Canada extends pandemic-related import program

March 22, 2021
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: MHRA resumes some onsite inspections; Kyprolis discount opens door to U.K. coverage; HHS delays Trump ‘Sunset’ rule.
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Regulatory actions for March 22, 2021

March 22, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Chiasma, Clarus, Crinetics, Lumos, Neurocrine, Strongbridge, Rezolute, Rhythm, Theratechnologies.
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