ICU Medical has received the US Food and Drug Administration (FDA) 510(k) clearance for its ChemoLock needlefree closed system transfer device (CSTD). The CSTD is approved for pharmacy applications (product code ONB), as well as patient ...
Tags: ICU Medical, FDA Approval
US-based PrintSure Digital Packaging has installed Xeikon's digital color press in a bid to support its growing digital printing business. PrintSure president Phil Edwards said that the company selected Xeikon digital color press because ...
Celgene has received approval from the US Food and Drug Administration (FDA) for its drug 'Abraxane' to treat patients with late-stage adenocarcinoma of the pancreas. Adenocarcinoma is a sub-type of exocrine tumors which accounts for ...
StelKast, a manufacturer and distributor of orthopedic implants for knee replacement and hip replacement, has received 510(k) clearance from the US Food and Drug Administration (FDA) to market EXp for the Proven Gen-Flex total knee system. ...
Tags: Stelkast, Total Knee System
The US Food and Drug Administration (FDA) has scheduled a meeting on 03 October 2013 to discuss QRxPharma's Moxduo new drug application (NDA) for the treatment of moderate to severe acute pain. The meeting is aimed at focusing on ...
Tags: Acute Pain Drug
Most of us have been exposed to tablets of all sizes- round, oval, disc, oblong, square, etc. and at some point of life, we've also thought of why these tablets have a particular shape and how are they made so perfect? For the latter part ...
The US Food and Drug Administration (FDA) has accepted for review the complete response submission made by Endo Health Solutions' subsidiary Endo Pharmaceuticals to the new drug application (NDA) for its testosterone undecanoate injection ...
Tags: Aveed Injection, Medicine
Therapeutic devices developer Abyrx has received 510(k) approval from the US Food and Drug Administration (FDA) for its new resorbable hemostatic bone putty called Hemasorb Plus that achieves hemostasis by mechanical tamponade. Hemasorb ...
CSL Behring has received approval from the US Food and Drug Administration (FDA) for a new 10g (50mL) vial size of Hizentra, an immune globulin subcutaneous (human) liquid drug. Hizentra, which is claimed to the first and only 20% ...
Tags: CSL Behring, Hizentra
Royal Philips Electronics has launched new Epiq premium ultrasound system designed to visualize deeper levels of anatomical detail and contrast resolution on patients of all types. Epiq, the new ultrasound system which features nSIGHT ...
The US Food and Drug Administration (FDA) has approved the third drug to be offered in the new BD Simplist line of ready-to-administer prefilled generic injectables. The third BD Simplist product to be introduced includes Ondansetron ...
Global health care company Fresenius Kabi USA has rolled out its Levofloxacin in 5% Dextrose injection in freeflex containers, designed for better infusion of solutions. Considering easy handling with improved safety and environmental ...
Tags: Fresenius Kabi, Freeflex Container
Octapharma USA, part of Swiss human protein products maker Octapharma Group, has announced the availability of Octaplas, a solvent/detergent treated pooled human plasma, in the country. Designed to reduce the risk of pathogen transmission ...
Tags: protein products, Octapharma
International specialty pharma company Meda has signed a definitive agreement to acquire Acton Pharmaceuticals, a specialty respiratory pharmaceutical company, in an all cash transaction. The proposed transaction, with a total potential ...
Tags: Pharmaceuticals, Meda
Advanced Bionics has obtained the US Food and Drug Administration (FDA) approval for its new Naída CI Q70 (Naída CI) sound processor which is now commercially available in the US. Advanced Bionics in collaboration with ...
Tags: Advanced Bionics, Sound Processor