MPR

FDA Cites Pouch Design and Labeling Deficiencies in Anaphylm CRL

The FDA has requested new human factors and pharmacology studies for Anaphylm sublingual film following deficiencies in original NDA packaging data.

FDA Strikes Off European Biotech Pharming's Immune Deficiency Drug For Expanded Use In Pediatric Patients

FDA issued a CRL to Pharming's Joenja child use filing, citing dosing concerns in lower-weight kids and testing issues.

Moment of Clarity Releases Educational Resource on SPRAVATO® Pricing Using Insurance

LONG BEACH, CA - January 16, 2026 - PRESSADVANTAGE - Moment of Clarity has published a new educational resource to help ...
Hosted on MSN

Are there any FDA-approved male enhancement pills?

This article was reviewed by Kelly Brown, MD. Ads for male enhancement supplements are everywhere. If you turn off your pop-up blocker for even a second, you’ll be bombarded with spots for “the best ...

Trace Biosciences Announces FDA IND Clearance for First Nerve-Specific Imaging Agent

"This IND clearance is a major milestone for Trace and validates more than a decade of scientific work focused on making nerves visible to surgeons," said Connor Barth, Ph.D., Co-Founder and CEO of ...
Healio

FDA approves updated label with new dosing guidance for inhaled insulin

The FDA has approved a label update for an inhaled insulin indicated for adults with type 1 or type 2 diabetes, according to ...
Migraine Again on MSN

Nurtec ODT: FDA approved as the only migraine medication for prevention and acute treatment

Discover how rimegepant (Nurtec ODT) works for both migraine treatment and prevention. Learn about the approved age range, dosage, and how long it takes to see results.

Las Vegas Eye Institute Introduces Ray-Traced LASIK: A New Era of Personalized Vision Correction

Henderson, NV - January 16, 2026 - PRESSADVANTAGE - Las Vegas Eye Institute announces the integration of Ray-Traced ...