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BioWorld - Wednesday, December 17, 2025
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Regulatory front for Jan. 29, 2020

Jan. 29, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory front for Jan. 28, 2020

Jan. 28, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Innate Immunotherapeutics, Australia’s Therapeutic Goods Administration
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Australia’s TGA proposes fee increases to implement recent drug, device reforms

Jan. 28, 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.
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Regulatory front for Jan. 28, 2020

Jan. 28, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Practice Fusion
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Biointellisense scores win at FDA with the clearance of its Biosticker

Jan. 28, 2020
By Liz Hollis
Biointellisense Inc. received good news from the U.S. FDA, which gave its nod to the company’s Biosticker on-body sensor for scalable remote care. The Biosticker allows for continuous monitoring of vital signs and actionable insights, delivered to clinicians from patients in the home setting. The goal is to help in the early detection of potentially avoidable complications.
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FDA continues to map out the regulatory road for gene therapies

Jan. 28, 2020
By Mari Serebrov
With four gene therapies already approved and more than 900 in development, the FDA has finalized six guidances and issued a draft guidance to clarify the rules of the road for developing and manufacturing the treatments. 
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Regulatory front for Jan. 28, 2020

Jan. 28, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Johnson & Johnson, Insys Therapeutics Inc.
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FDA approves Trijardy XR for type 2 diabetes

Jan. 28, 2020

Regulatory front for Jan. 27, 2020

Jan. 27, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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Gt Medical gains expanded indication in the U.S. for Gammatile therapy

Jan. 27, 2020
By Liz Hollis
Tempe, Ariz.-based Gt Medical Technologies Inc. has won the U.S. FDA’s nod for an expanded indication for Gammatile therapy. With this decision, patients with newly diagnosed malignant brain tumors now are eligible to receive the FDA-cleared surgically targeted radiation therapy. Gammatile therapy offers an option vs. waiting several weeks for surgical wound healing before beginning treatment. Previously, the therapy was available for individuals with recurrent brain tumors.
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