Game on, Pfizer: Merck's Vaxneuvance boosts pneumococcal vaccine fight with coveted pediatric nod (Fierce)
Athira’s alternative Alzheimer’s approach runs into a PhII brick wall (Endpoints)
AbbVie walks away from Morphic deal in aftermath of safety signal in preclinical testing (Endpoints)
NICE opts to reject Acorda’s MS drug Fampyra (PharmaTimes)
Merck scoops up new chief marketing officer from Biogen's neurology business (Endpoints)
Doudna research team finds CRISPR-Csm delivery potentially outperforms RNAi, Cas13 (Endpoints)
Medtech
FDA adds Class I tag to Dräger’s recall of 36K ventilator filters (Fierce)
FDA opens consultation on tissue removal devices to reduce cancer risk (MedtechDive)
Medtronic reinforces spine surgery portfolio with FDA nod for ligament-augmenting implant (Fierce)
GE Healthcare debuts wireless, wearable hospital patient monitor (Fierce)
Government, Regulatory & Legal
Fraud trial against Elizabeth Holmes’ partner at Theranos nears end (CNBC)
Two Florida Men Charged With Profiting Off Fake Prescriptions (NYTimes)
Philips Knew Of CPAP Foam Issues In 2015, Device Users Say (Law360)
Senate lawmakers introduce a bill to help the FDA and the U.S. Patent Office coordinate (STAT) (Law360)
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The US Food and Drug Administration (FDA) issued final guidance on 13 August regarding the types and timelines for formal meetings that sponsors can request during the development of new drugs and biological products.
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