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BioWorld, Regulatory
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Gavel and scales

Securities class action suits a growing fact of life for life sciences

Jan. 23, 2020
By Mari Serebrov
Whether large or small, or based in the U.S. or abroad, life sciences companies are an increasingly attractive target for shareholder suits. The number of securities fraud class action suits filed in the U.S. in 2019 across all industries totaled 404, just one more than the 403 cases filed in 2018 and down from the peak of 412 in 2017, according to a new Dechert LLP report.
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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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