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BioWorld - Friday, June 26, 2026
Home » Topics » Regulatory

Regulatory
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Regulatory actions for Oct. 5, 2021

Oct. 5, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: AB Science, Allovir, Arcutis, Astrazeneca, Biontech, Celltrion, Coherus, Cour, Daiichi, Heron, Himalaya, Janssen, Kite, Moderna, Novartis, Pfizer, Relmada, Turning Point, Zosano.
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FDA icons

FDA clears Siemens Healthineers photon-counting CT device

Oct. 4, 2021
By Catherine Longworth
The FDA has granted clearance of Siemens Medical Solutions Inc.’s photon-counting computed tomography (CT) scanner, Naeotom Alpha. The new diagnostic imaging device uses a photon-counting detector that measures individual X-rays that pass through a patient's body, as opposed to current systems that use detectors that measure the total energy contained in X-rays at once. The scanner then transforms the information from the X-ray photons into a detailed three-dimensional image, which can be used by physicians to assist diagnosis or treatment preparation planning.
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Regulatory actions for Oct. 4, 2021

Oct. 4, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Labcorp.
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TGA recognizes COVID-19 vaccines for travel purposes

Oct. 4, 2021
In addition to the four COVID-19 vaccines it has provisionally approved, Australia’s Therapeutic Goods Administration (TGA) is recommending that two more vaccines – Sinovac Biotech Ltd.’s Coronavac and Astrazeneca plc-Serum Institute of India’s Covishield – be considered “recognized vaccines.”
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EMA assessing tumor risk with use of gynecology drugs

Oct. 4, 2021
At the request of France’s ANSM, the EMA is reviewing drugs containing nomegestrol or chlormadinone to assess the risk of meningioma with their use.
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Generic firms agree to pay $450M to resolve price-fixing allegations

Oct. 4, 2021
By Mari Serebrov
Three generic drug companies have agreed to pay a total of nearly $450 million to resolve U.S. Department of Justice (DoJ) price-fixing allegations.
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340B litigation grows with PhRMA challenge to state law

Oct. 4, 2021
By Mari Serebrov
In the latest skirmish over who can get the 340B discounts on prescription drugs that are supposed to help qualifying U.S. providers offer charity care, the Pharmaceutical Research and Manufacturers of America (PhRMA) is challenging a recently passed Arkansas law that seeks to regulate drug manufacturers’ participation in the federal drug pricing program.
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EMA icons

EMA reverses course on COVID-19 boosters

Oct. 4, 2021
By Nuala Moran
LONDON – The EMA has changed its stance on booster doses of the Pfizer Inc./Biontech SE COVID-19 vaccine and said they “may now be considered” at least six months after the second dose for people ages 18 and over.
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Regulatory actions for Oct. 4, 2021

Oct. 4, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: BMS, Humanigen, Kite, Omeros, Xbrane.
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Brain and encephalography

Wyss Center’s cloud-based brain monitoring software receives CE mark

Oct. 1, 2021
By Catherine Longworth
A cloud-based web application for long-term brain monitoring has received a CE mark to support personalized management of neuro-disorders such as epilepsy. Developed by Swiss neuroscience research organization Wyss Center, Epios Cloud displays and reviews electroencephalogram (EEG) recordings made by EEG devices using scalp and sub-scalp electrodes, heart rate and accelerometer measurements.
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