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BioWorld - Saturday, August 1, 2026
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United Kingdom flag, map

Post-Brexit med-tech legislation takes on life of its own in U.K.

Feb. 10, 2021
By Nuala Moran
LONDON – It began life as a legal tidy-up of post-Brexit regulatory issues, but the Medicines and Medical Devices bill that emerged from its final reading last week is in a significantly different form. Most notably, the bill legislates for the creation of a national register of all implantable medical devices and the appointment of a patient safety commissioner to act a single port of call and advocate for patients when devices fail.
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Regulatory front for Feb. 10, 2021

Feb. 10, 2021
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: HHS posts request for information for Lyme diagnostics; NICE: Stak device backed by one 35-enrollee study.
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Regulatory actions for Feb. 10, 2021

Feb. 10, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Alveo, Cardiacsense, Kantaro, Surgical Planning Associates, Visby.
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EC’s Aspen decision provides guidance on excessive prices

Feb. 10, 2021
By Mari Serebrov
In its first decision on excessive drug pricing, the European Commission (EC) accepted a commitment Feb. 10 from Aspen Pharmacare Holdings Ltd. to immediately drop the price of six essential cancer drugs in Europe by an average of 73% and to continue to supply the drugs for at least the next five years.
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Bamlanivimab and etesevimab

FDA grants EUA for Abcellera-Junshi-Lilly COVID-19 treatment

Feb. 10, 2021
By Lee Landenberger
Another monoclonal antibody therapy has entered the pandemic fray with the FDA granting emergency use authorization (EUA) for bamlanivimab (LY-CoV555) 700 mg and etesevimab (JS016 or LY-CoV016) 1,400 mg as a cocktail for treating mild to moderate COVID-19 in patients aged 12 and up at high risk for progressing to severe COVID-19 and/or hospitalization.
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Regulatory front for Feb. 10, 2021

Feb. 10, 2021
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for Feb. 10, 2021

Feb. 10, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbvie, Adaptive Phage, AIM Immunetech, Astrazeneca, Biontech, Eli Lilly, I-Mab, Merck, Panbela, Pfizer, RDIF, Regeneron, Sanifit, Sanofi, Takeda, Vico.
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Generic drugs and bottle

Savings from complex generics remain elusive in U.S.

Feb. 10, 2021
By Mari Serebrov
Among the low-hanging fruit for pruning back U.S. drug prices is the development of generics referencing complex drugs, a category that includes drug-device combination products and nonbiologic drugs with a complex molecular base, route of administration or formulation, such as abuse-deterrent opioids.
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FDA grants EUA for etesevimab and bamlanivimab for mild to moderate COVID-19

Feb. 10, 2021

FDA approves Libtayo for advanced basal cell carcinoma

Feb. 10, 2021
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