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BioWorld - Friday, February 6, 2026
Home » Topics » Regulatory

Regulatory
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FDA Approved road sign

Angle of ketorolac attack yakked as Baudax hails Anjeso pesos

Feb. 21, 2020
By Randy Osborne
During a conference call with investors, Baudax Bio Inc. CEO Gerri Henwood let out an exuberant “woohoo!” to celebrate the FDA’s approval – after two turndowns and much haggling over data – of Anjeso (meloxicam) for moderate to severe pain. Echoing her sentiment was Piper Sandler analyst David Amsellem. “It’s nice to see the pain division finally get this one right,” he said.
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Regulatory front for Feb. 21, 2020

Feb. 21, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Ferring Pharmaceuticals.
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Opdivo approved in Japan for advanced esophageal cancer

Feb. 21, 2020

Regulatory front for Feb. 20, 2020

Feb. 20, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Ethicon, Intuitive Surgical.
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Map of Europe

MDMA’s Leahey says harmonization great, but EU transition a more pressing concern

Feb. 20, 2020
By Mark McCarty
The 2.3% medical device tax is a thing of the past, and now Medicare coverage is one of the issues that is front and center for the Medical Device Manufacturers Association. MDMA President and CEO Mark Leahey told BioWorld also that while member companies are keen on regulatory harmonization, the struggles in standing up the new European regulatory framework is a far more pressing concern.
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Australian flag on laptop screen with health professional

Australia lays out evidence requirements for device marketing authorization applications

Feb. 20, 2020
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Goods Administration (TGA) has issued a draft guidance to help sponsors better understand the evidence requirements for market authorizations for medical devices, including in vitro diagnostics (IVDs) and software as a medical device (SaMD).
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Map, flag of India

India gathers more med-tech products under its drug control regulations

Feb. 20, 2020
By David Ho
HONG KONG – India’s central government has finally placed most med-tech devices into the category of ‘drugs,’ subjecting them to control under the Drugs and Cosmetics Act, 1940.
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Biosimilar drugs

FDA prepares for NDA-to-BLA deeming day

Feb. 20, 2020
By Mari Serebrov
With deeming day a little more than a month away, the FDA is taking final steps to ease the transition of simple proteins approved as new drug applications (NDAs) to biologic license applications (BLAs). The March 23 change will open drugs such as insulin and various hormones to new competition, likely bringing in the next wave of biosimilars. And this time, interchangeability could be riding the crest.
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Regulatory front for Feb. 20, 2020

Feb. 20, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Vertex Pharmaceuticals.
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U.S. EPA building

Advamed questions EPA methodology for risk associated with ethylene oxide

Feb. 20, 2020
By Mark McCarty
The response from industry regarding the Environmental Protection Agency’s (EPA) draft rule for ethylene oxide (EtO) varied considerably, but the Advanced Medical Technology Association (Advamed) argued a fundamental methodological point in its comments to the docket. Advamed’s Ruey Dempsey said the EPA approach to determining safe levels of EtO relies on “a single epidemiological study,” an approach Dempsey said has drawn fire from the National Academies of Science.
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