Cresset’s new India site will support the growing demands of Cresset’s APAC customer base
NULIBRY is a first-in-class synthetic cPMP substrate replacement therapy to reduce the risk of mortality in patients with MoCD Type A
Vericiguat works on a pathway not currently targeted by existing heart failure treatments
The approval marks a significant milestone for the American pharmaceutical company in the field of UC
Centhaquine is a resuscitative agent presently indicated for the treatment of hypovolemic shock by DGCI
These approvals mark significant progress for Venus Remedies in expanding its market presence
This agreement paves the way for the introduction of YESAFILI into the Canadian market
The agreement licenses the company to launch in the United States, in February 2025, once approved by the U.S. FDA
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