pharmadog
News
when
  • Latest
  • Archive
by source
  • All Sources
  • Sources Page
Jobs
department
  • Clinical
  • Regulatory
  • Medical Affairs
  • Commercial
  • R&D / Discovery
  • Biostatistics / Data
  • Manufacturing / CMC
  • Market Access
therapeutic area
  • Oncology
  • Immunology
  • Neuroscience
  • Cardiovascular
  • Metabolic
  • Rare Disease
  • Infectious Disease
location & type
  • Remote Only
  • US Only
  • California
  • Massachusetts
  • Internships
  • Phase 3 Roles
  • All Jobs →
Sign InSubscribe
pharmadog

fetch the data · sniff the signal

Discover
  • Jobs
  • News
Hubs
  • Topics
  • Patent cliff
  • Publications
Tools
  • Compare
  • Search
  • Bookmarks
Trust
  • About
  • Sources
  • Contact
Legal
  • Privacy
  • Terms
  • Pricing

© 2026 pharmadog.xyz

made by humans and a good dog

  • home
  • jobs
  • news
  • search
fda press·4h ago·1 min read
save

FDA approves first freeze-dried plasma product for U.S. use

Jul 29, 2026·read at fda press ↗ApprovalPositive

The FDA has licensed Ezplaz Freeze Dried Plasma (FDP), marking the first freeze-dried plasma product cleared for use in the United States.

The product is intended for adult patients who need plasma when other plasma products are unavailable, such as in combat zones, disaster sites, rural or other austere settings. It can be stored at room temperature, remains stable through temperature changes, and can be reconstituted quickly, offering faster access compared with conventional frozen plasma that requires thawing.

Ezplaz is derived from a single unit of fresh frozen plasma and is offered in Group AB and Group A low-titer anti-B blood types to reduce risk when a patient’s blood type is unknown. It is packaged in a plastic bag rather than a glass bottle, lowering breakage risk during transport.

source

This writeup was produced by pharmadog from original reporting by fda press.

Original headline: “FDA Licenses First-Ever Freeze-Dried Plasma Product in the U.S.”

read at fda press ↗
564 words · retrieved 1h ago
sharex / twitterlinkedin

comments(0)

5-min edit window · permanent after that
sign in to leave a comment · permanent archive after 5 minutes
no comments yet — first sniff?

companies & drugs in this story

no entities indexed yet

related stories

  • Jul 22FDA Announces First Participant Selected for TEMPO for Digital Health Devices Pilotfda press
  • Jul 22FDA Takes Further Steps to Remove Outdated Authorizations for Color Additives in Foodfda press
  • Jul 17FDA Approves First Oral PCSK9 Inhibitor to Lower LDL Cholesterol in Adults with High Cholesterolfda press
  • Jul 15FDA Issues Emergency Use Authorization for Drug for Short-Term Prevention of New World Screwworm in Horsesfda press
  • Jul 10FDA Proposes Rule to Modernize Drug Manufacturing Registrationfda press