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Home » Topics » BioWorld, Regulatory

BioWorld, Regulatory
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Regulatory actions for Nov. 17, 2020

Nov. 17, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Alkermes, Apellis, Azurrx, BMS, CNS, Cytodyn, Inovio, Istari, Kiniksa, Moderna, Plx, Praxis, Redhill, UCB, Verrica, Viiv.
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Skeptical OIG issues fraud alert about speaker programs

Nov. 16, 2020
By Mari Serebrov
If the Office of Inspector General (OIG) for the U.S. Department of Health and Human Services has its way, one of the casualties of the COVID-19 pandemic would be the in-person speaker programs many drug and device companies sponsor. The OIG issued a special fraud alert Nov. 16 questioning the need for such events in which health care professionals are often paid a hefty honorarium or fee to provide colleagues with information that’s readily available online and in the labeling of a drug or device.
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Illustration of red blood cells traveling in the arteries

A CRL for sutimlimab is Sanofi’s Friday 13th bad luck charm

Nov. 16, 2020
By Lee Landenberger
The FDA has issued Sanofi SA a complete response letter (CRL) regarding its complement pathway inhibitor sutimlimab, citing deficiencies found during a pre-license inspection of a third-party manufacturing facility.
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Regulatory actions for Nov. 16, 2020

Nov. 16, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: 3D, Agilent, Alphamab, Amylyx, Artelo, Aruvant, Boehringer, Cytodyn, Dicerna, Eisai, Exegi, Innovation, Insmed, Kiniksa, Jounce, Lilly, Lupin, Merck, Mindmed, Neoimmunetech, Neuronasal, Sanofi, Tracon.
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Regulatory front

Vaccine, diagnostic developers targeted by cyberattacks

Nov. 16, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: Lawmakers protest latest 340B scheme; Groups make case for extending sequester moratorium; More $$ needed for global vaccine effort; Russia extends COVID-19 drug, device program.
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Regulatory actions for Nov. 13, 2020

Nov. 13, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aerie, Agios, Amgen, Bayer, Biomarin, Boehringer Ingelheim, Chiesi, Heron, Innate, Menari, Moderna, Roche, Samsung, Shionogi, Sobi, UCB, Viiv.
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Vaccine administration

Anvisa restarts trials for Sinovac’s COVID-19 vaccine

Nov. 12, 2020
By Sergio Held and Alfred Romann
BOGOTA, Colombia and VANCOUVER, Canada – Anvisa, Brazil’s health care surveillance agency, re-started phase III trials for Coronavac, the COVID-19 vaccine candidate developed by China-based Sinovac Biotech Ltd., after a suspension of just two days. “Anvisa understands that it has sufficient subsidies to allow the resumption of vaccination,” the regulator said on Nov. 11. Anvisa said it plans to continue monitoring “the possible relationship of causality” between an unexpected serious adverse event and the vaccine.
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Regulatory front

NICE news for patients with CLL, TTP

Nov. 12, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: WHO maps end of the road for some tropical diseases; MHRA updates import licensing guidance.
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Regulatory actions for Nov. 12, 2020

Nov. 12, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Alzecure, Apollomics, Bavarian Nordic, Halozyme, Janssen, Mycovia, Neonmind, Valeo, Vasomune.
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Regulatory front

ICER adjusts Veklury price models – again

Nov. 11, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: MHRA advises on minimizing trial disruptions.
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