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BioWorld - Tuesday, July 14, 2026
Home » Topics » Regulatory

Regulatory
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Shipping container with flag of China

Beijing export officials using black, whitelists to determine exportability of test kits

June 10, 2020
By Mark McCarty
The impact of the COVID-19 pandemic has reached into quarters that are not historically problematic for makers of diagnostics, including China’s import and export practices for test kits. According to one caller on an FDA diagnostic town hall, export officials in China have a blacklist and a whitelist for test kits, but there is some dispute as to whether kits that are eligible for distribution in the U.S. can get off the blacklist unless that kit is specifically called out via the emergency use authorization (EUA) program.
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Components of the Go-2 system

Gtx Medical receives breakthrough device designation for implanted spinal stimulation system

June 10, 2020
By Annette Boyle
The U.S. FDA granted Gtx Medical BV a breakthrough device designation for its implantable Go-2 Targeted Epidural Spinal Stimulation (TESS) system. The device enabled patients who had sustained traumatic spinal cord injuries to regain voluntary control over previously paralyzed muscles and walk again four or more years after paralysis, according to a study previously published in Nature.
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Regulatory front for June 10, 2020

June 10, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Advamed.
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Regulatory actions for June 10, 2020

June 10, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Chromacode, Illumina, Quidel.
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India posts draft rules for compassionate use of unapproved drugs

June 10, 2020
By David Ho
HONG KONG – India’s Ministry of Health and Family Welfare (MOHFW) has drafted rules for the manufacturing, import and the compassionate use of unapproved drugs in the treatment of patients.
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Regulatory actions for June 9, 2020

June 10, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: 4web Medical, Atomic Blue, Dexcom, Hangzhou Biotest Biotech, Incelldx, Seasun Biomaterials, Sekisui Diagnostics, Vasoptic Medical.
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Regulatory actions for June 10, 2020

June 10, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Bacainn, Curis, F2G, Fulcrum, Pharnext, Redhill, Rezolute, Vertex.
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Beigene’s FDA-cleared BTK inhibitor Brukinsa approved in China

June 9, 2020
By Elise Mak
Chinese biotech firm Beigene Ltd. said its second-generation BTK inhibitor, Brukinsa (zanubrutinib), has won approval in China for two indications, entering a market dominated by Imbruvica (ibrutinib, Johnson & Johnson/Abbvie Inc.). The NDA approval came eight months after Brukinsa’s clearance in the U.S.
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Architectural pillars

Regulatory front for June 9, 2020

June 9, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Biomedical Advanced Research and Development Authority, Biotechnology Innovation Organization, Council of State Bioscience Associations, FDA, HHS, U.S. Department of Agriculture, U.S. House, U.S. House Select Subcommittee on the Coronavirus Crisis, U.S. Senate.
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Regulatory front for June 9, 2020

June 9, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Intersect ENT.
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