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BioWorld - Friday, July 10, 2026
Home » Topics » Regulatory

Regulatory
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FDA’s artificial intelligence paper prompts concerns regarding practicability

July 6, 2020
By Mark McCarty
The comment period has closed on the U.S. FDA’s discussion draft for artificial intelligence (AI) in medical devices, a paper that attracted the attention of medical societies and regulated industry. One of the questions posed by industry was whether the FDA is in a position to deal with the massive volumes of data developers would have to disclose to the agency, creating concern that such disclosures would amount to little more than an obligatory and useless data dump.
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Gallant devices with mobile app

Abbott scoops up win at FDA for Gallant ICD, CRT-D devices

July 6, 2020
By Liz Hollis
The U.S. FDA has given its nod to Abbott Laboratories' next-generation Gallant implantable cardioverter defibrillator (ICD) and cardiac resynchronization therapy defibrillator (CRT-D) devices. The Gallant system pairs with Abbott's secure Mymerlinpulse, an iOS- and Android-compatible mobile smartphone app that aims to streamline communication between doctors and their patients.
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Regulatory front for July 6, 2020

July 6, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Aetna, Arrow International, BD, Erba Diagnostics, Eternity Healthcare.
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Regulatory actions for July 6, 2020

July 6, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbott, BD, Centogene, Cochlear, Inmode.
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Regulatory actions for July 6, 2020

July 6, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: ADC, Adial, Ascendis, CSL Behring, Daiichi Sankyo, Esperare Foundation, Gilead, Medivir, Mesoblast, Mylan, Napo, Sinovac, Viiv.
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FDA approves Byfavo injection for the induction and maintenance of procedural sedation

July 3, 2020

FDA approves Rukobia for the treatment of adults with multidrug-resistant HIV-1 infection

July 3, 2020
Product image

Carag secures IDE approval for Bioresorbable Septal Occluder

July 2, 2020
By Annette Boyle
Carag AG received investigational device exemption (IDE) approval from the U.S. FDA for its Carag Bioresorbable Septal Occluder (CBSO). The device is the first transcatheter septal occluder with a nonmetal, bioresorbable framework. The Baar, Switzerland-based company plans a "swift start" for a staged study trial in the U.S. with 250 patients, Carag's CEO Jérôme Bernhard told BioWorld.
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Regulatory front for July 2, 2020

July 2, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Agendia, Teva.
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Regulatory actions for July 2, 2020

July 2, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Life Whisperer, Phosphorus, Sagico, Spinal Elements.
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