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BioWorld - Tuesday, December 23, 2025
Home » Topics » Regulatory

Regulatory
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Shuren cites need for flexibility, says regulatory Legos the prescription

Sep. 27, 2019
By Mark McCarty
BOSTON – The 2019 Medtech Conference included the annual FDA town hall session, and Jeff Shuren, director of the agency's device center, said the pace of scientific change is outstripping the agency's ability to keep up. Shuren said the solution might be "regulatory Legos," an approach that might eliminate the need to go to Congress for new statutory authorities every time device makers carve open a new technological frontier.
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Industry warns Labour's plan to cut drug prices would discourage U.K. innovation

Sep. 26, 2019
By Nuala Moran
LONDON – The industry has hit out at a proposal by the U.K.'s opposition Labour party to create a state-owned generic drugs company to supply the National Health Service and to force companies to cut the cost of expensive proprietary products.
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Politics overriding congressional Rx pricing fix

Sep. 26, 2019
By Mari Serebrov
Wednesday's House subcommittee hearing on H.R. 3, which tasks Medicare with directly negotiating prescription drug prices in the U.S., may have been an exercise in futility. Although both Republicans and Democrats in Congress still agree that something has to be done to lower drug prices, they are beyond compromise on key aspects of H.R. 3, the Lower Drug Costs Now Act.
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China's state machine is set to drive innovation, but needs more than just drug law reforms

Sep. 25, 2019
By Elise Mak
SUZHOU, China – A recent revision to China's legal infrastructure for the pharma industry represents a concrete step toward bolstering domestic biotech innovation, said stakeholders gathered at last weekend's China Biomed Innovation and Investment Conference.
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More approvals by FDA: Rare disease, oncology and HKEX remain the focus

Sep. 25, 2019
By Elise Mak
SUZHOU, China – The global biotech market continues to look promising and Chinese companies are taking notice as they lay the foundation for new advances.
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Product regulatory actions for Sept. 23, 2019

Sep. 24, 2019

FDA lays framework for engaging patients in device clinical trials

Sep. 24, 2019
By Meg Bryant
BOSTON – The FDA's Center for Device and Radiological Health (CDRH) released draft guidance on Monday aimed at encouraging the use of patient input in medical device clinical trials and helping sponsors understand how they can use patient engagement to improve the design and conduct of investigations.
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Is Brazil moving toward a med-tech price cap?

Sep. 24, 2019
By Sergio Held
BOGOTA, Colombia – Last month, Anvisa, Brazil's health surveillance agency, approved a proposal that makes it mandatory for the agency to monitor the prices of medical implants, a category that, in Brazil, includes orthoses, prostheses and special materials. Is this the beginning of a price capping era for medical devices in the Latin American giant?
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Regulatory front

Sep. 24, 2019

Crysvita approved in Japan for FGF-23-related hypophosphatemic rickets and osteomalacia

Sep. 23, 2019
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