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BioWorld - Sunday, April 5, 2026
Home » Topics » Regulatory

Regulatory
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Colombia expands price caps: 2,487 drugs now have price regulation

Feb. 12, 2020
By Sergio Held
BOGOTA, Colombia – As part of an effort to further control drug costs, Colombia set price caps on 770 drugs in late January. The move takes the total of price-regulated drugs in the Latin American country to 2,487. The new caps on drug prices apply to a broad range of products from generics to biosimilars and to biologics such as ranibizumab, trastuzumab, vedolizumab, secukinumab and pembrolizumab, among dozens of others.
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Regulatory front for Feb. 12, 2020

Feb. 12, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Reactants ignite, China syndrome melts down FDA drug-quality meeting

Feb. 11, 2020
By Randy Osborne
A half-day open meeting intended to examine “how the public perceives and values pharmaceutical quality,” convened by the Robert J. Margolis Center for Health Policy at Duke University in cooperation with the FDA, included a rundown of the agency’s oversight program, results of surveys to measure viewpoints of patients and providers – and tart commentary from a two-member “reactant panel.”
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Architectural pillars

Regulatory front for Feb. 11, 2020

Feb. 11, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Aurolife, CDC, Central Drugs Standard Control Organisation, FDA, Glaxosmithkline, National Institute of Allergy and Infectious Diseases, Sanofi, U.S. Court of Appeals, World Health Organization.
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Regulatory front for Feb. 11, 2020

Feb. 11, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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MITA urges FDA to make numerous technical changes to performance draft for MRI coils

Feb. 11, 2020
By Mark McCarty
The Dec. 9, 2019, FDA draft guidance spelling out performance criteria for magnetic resonance coils seemed to take up a relatively simple matter, but industry’s response suggested otherwise. The Medical Imaging & Technology Alliance (MITA) recommended that the agency undertake nearly two dozen changes to the draft, including a change to the title to indicate that the scope of the guidance is limited to receive-only MRI coils.
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Logicbio shares sink as FDA hold delays plans to launch phase I/II trial

Feb. 11, 2020
By Michael Fitzhugh
Pediatric gene editing specialist Logicbio Therapeutics Inc. has revealed an FDA clinical hold on a planned phase I/II trial of its lead candidate, LB-001, an investigational therapy for rare inherited metabolic disorder methylmalonic acidemia (MMA).
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Varian receives FDA nod for Ethos therapy

Feb. 11, 2020
By Liz Hollis
Palo Alto, Calif.-based Varian Medical Systems Inc. has won the U.S. FDA’s nod for its Ethos therapy, an artificial intelligence (AI)-driven holistic solution that is aiming to transform cancer care. This solution is designed to deliver an entire adaptive treatment in a typical 15-minute slot and is intended to put the patient at the center of care, noted Chris Toth, president of Varian Oncology Systems.
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Fate of California law could dictate future of Rx patent settlements

Feb. 11, 2020
By Mari Serebrov
The Association for Accessible Medicines (AAM) is garnering support in its Ninth Circuit challenge to a new California law that seemingly thumbs its nose at a 2013 U.S. Supreme Court ruling on so-called pay-for-delay patent settlements.
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Regulatory front for Feb. 11, 2020

Feb. 11, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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