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BioWorld - Wednesday, March 18, 2026
Home » Topics » Regulatory

Regulatory
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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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Patents, regulations and tech transfer: Challenges for the biotech sector in LatAm

July 2, 2020
By Sergio Held
CAJICA, Colombia – The Latin American biotech sector is scrambling in the midst of the COVID-19 pandemic, not only in coping with the outbreak, but also in finding the path to the future, while avoiding the pitfalls and looking for new opportunities ahead.
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Japan’s MLWH ends June with string of approvals, looks set for busy 2H 2020

July 2, 2020
By Gina Lee
HONG KONG – Japan’s Ministry of Health, Labour and Welfare (MHLW) ended the first half of 2020 by handing out a flurry of approvals to both domestic and international companies across a wide spectrum of indications.
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Regulatory front for July 2, 2020

July 2, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for July 2, 2020

July 2, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Acacia, Beigene, Biophytis Eusa, Geron, Metvital, Mundipharma, Napp, Rhythm.
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European Commission approves Janssen's Ebola vaccine regimen

July 2, 2020
Product image

CMS steers closer to coverage of secondary mitral regurgitation in draft coverage rewrite

July 1, 2020
By Mark McCarty
The U.S. Centers for Medicare and Medicaid Services (CMS) posted the much-anticipated draft do-over of the mitral valve repair device coverage memo, and in the process renamed the policy the mitral valve transcatheter edge-to-edge repair (TEER) national coverage memo.
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Knee implant in skeleton model

FDA greenlights Engage Surgical’s cementless partial knee system

July 1, 2020
By Meg Bryant
Orthopedic implant startup Engage Surgical has received 510(k) clearance from the FDA for its Engage Partial Knee system, the only cementless partial knee implant available in the U.S. The company is introducing the product via a limited release to select surgical centers.
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Regulatory front for July 1, 2020

July 1, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Advamed.
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