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BioWorld - Tuesday, June 16, 2026
Home » Topics » Regulatory, BioWorld

Regulatory, BioWorld
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Australia’s TGA proposes fee increases to implement recent drug, device reforms

Jan. 23, 2020
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Goods Administration (TGA) is seeking input from industry stakeholders on a proposal to increase its fees to cover projected deficits this year. The proposal outlines three options.
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Regulatory front for Jan. 23, 2020

Jan. 23, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Insys
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Regulatory front for Jan. 22, 2020

Jan. 22, 2020
The latest global regulatory news, changes and updates affecting biopharma: Aegerion Pharmaceuticals Inc., Alexion Pharmaceuticals Inc., Insys Therapeutics Inc.
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Horizon wins FDA approval for thyroid eye disease drug Tepezza

Jan. 21, 2020
By Michael Fitzhugh
About a month-and-a-half earlier than expected, Horizon Therapeutics plc has won FDA approval for teprotumumab in thyroid eye disease (TED), a progressive autoimmune condition that disproportionately affects women.
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Health professional recording info from patient

Many sponsors still not publishing clinical data, despite new requirements, study finds

Jan. 21, 2020
By Nuala Moran
LONDON – Three years after the implementation of new U.S. legislation requiring clinical trials to report results within 12 months of completion, more than half are not published on time and compliance is not improving.
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Regulatory front for Jan. 21, 2020

Jan. 21, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Blue heart and data grid

Novo's Ozempic gets FDA go-ahead to expand label for reducing MACE

Jan. 17, 2020
By Michael Fitzhugh
Novo Nordisk A/S' Ozempic, a once-weekly injectable version of the company's glucagon-like peptide-1 (GLP-1) receptor agonist, semaglutide, first FDA-approved in late 2017, has won the agency' approval for a new indication: reducing the risk of major adverse cardiovascular events (MACE) in adults with type 2 diabetes (T2D) and known heart disease.
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China promotes real-world evidence in R&D and approval with new guidelines

Jan. 16, 2020
By Elise Mak
BEIJING – China has released guidelines to promote the use of real-world evidence (RWE) in drug development and reviews.
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Regulatory front for Jan. 16, 2020

Jan. 16, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory front for Jan. 15, 2020

Jan. 15, 2020
The latest global regulatory news, changes and updates affecting biopharma.
Read More
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