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BioWorld - Saturday, May 2, 2026
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Regulatory front for Sept. 15, 2020

Sep. 15, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Biotechnology Innovation Organization, FDA, Institute for Clinical and Economic Review, Medicines and Healthcare Products Regulatory Agency.
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Regulatory front

FDA releases guidance on COVID-19, geriatric labeling, EoE

Sep. 15, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: NIH adds funding to Latino Alzheimer’s research; Sprout warned for Addyi promotion; Scripps to pay $10M over use of NIH grants.
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Regulatory actions for Sept. 15, 2020

Sep. 15, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aerie, Amryt, Apellis, Ardelyx, Astrazeneca, BMS, Boehringer, Epimab, Equillium, Gensight, Gilead, Kiniksa, Lilly, Mateon, Matinas, Novartis, Plus, Takeda, Zynerba.
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Map of China

Hainan urgent device program underway, but complications await unwary device makers

Sep. 14, 2020
By Mark McCarty
China’s provincial government for Hainan Province has two sets of medical devices going through the urgent medical device needs program, but leveraging this program for regulatory approval in China is still no small undertaking. One complication is that any real-world evidence gathered in Hainan might not suffice for nationwide regulatory approval, but patient recruitment is also difficult.
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Man wearing Keeogo about to climb stairs

B-Temia gains traction with 510(k) clearance for mobility device

Sep. 14, 2020
By Annette Boyle
B-Temia Inc.’s Keeogo mobility device is on the move in the U.S. now that it has received 510(k) clearance from the U.S. FDA. Unlike currently available exoskeletons that move for patients, the Keeogo (keep on going) Dermoskeleton system amplifies signals from patients who can initiate movement but need additional assistance.
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Charmless: Third CRL for Mallinckrodt’s terlipressin

Sep. 14, 2020
By Lee Landenberger
Mallinckrodt plc’s decade-long frustration with getting approval for its vasopressin analogue selective for V1 receptors, terlipressin, for use in hepatorenal syndrome type 1 continues as the FDA issued the company a third complete response letter (CRL) for the drug.
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Regulatory front for Sept. 14, 2020

Sep. 14, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Becton Dickinson.
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Regulatory actions for Sept. 14, 2020

Sep. 14, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbott, B-Temia, Fitbit, Micron Medical.
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Regulatory front

Adcom: ADF offers no meaningful reduction in overall Oxycontin abuse

Sep. 14, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: FDA advises on getting back to business as usual; ICER evidence report targets ulcerative colitis treatments.
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Regulatory actions for Sept. 14, 2020

Sep. 14, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Ascentage, Cycle, Essa, Gan & Lee, Gannex, Kiadis, Mateon, Novartis, Pharmacyte, Regeneron, Reven, Sanofi, SK, Seneca, Supernus, Vaxart, Vertex, Ziopharm.
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