Insurance broker Wells Fargo Insurance has introduces two new products, namely revENSURE and ANDAfend, from its Professional Risk Group, Intellectual Property Risk Mitigation Practice (IPRMP) to help protect revenues or royalties from ...
Tags: Insurance, Intellectual Property
Hansen Medical has enrolled first patients for ARTISAN-AF clinical trial to evaluate the use of Artisan family of control catheters with its Sensei X robotic catheter system for treatment of atrial fibrillation. The robotic catheter ...
Tags: Hansen Medical, Clinical Trial
Quidel, a US-based virology assays and molecular diagnostic systems provider, has received 510(k) clearance from the US Food and Drug Administration (FDA) for its Sofia hCG fluorescent immunoassay for use on the Sofia Analyzer. It is used ...
Tags: FDA Clearance, HCG Fluorescent
Medtronic, a US-based developer of medical devices, has introduced its new implantable neurostimulation systems, also called spinal cord stimulation (SCS) systems, for use in the treatment of chronic, intractable back and limb pain that are ...
The US Food and Drug Administration (FDA) Ophthalmic Devices Advisory Panel is scheduled to decide on Ocular Therapeutix’s premarket approval application for the ReSure Sealant in September and may suggest some recommendations. ...
Tags: Ophthalmic Devices, Health
LDR has received a letter of approval from the US Food and Drug Administration (FDA) for commercial sale and distribution of its Mobi-C Cervical Disc (Mobi-C), for one-level indications in the US. The Mobi-C is designed for cervical disc ...
Tags: Mobi-C Cervical Disc
India-based Torrent Pharma’s US subsidiary has announced the recall of the company’s anti-psychotic drug Olanzapine 10mg tablets from the US market due to a packaging issue. Torrent manufactured the drug for Prasco Labs in the ...
Tags: Torrent Pharma, Packaging Issue
Evonik Industries is now significantly expanding precipitated silica capacity at its Maptaphut site in Thailand. Funded by an investment in the lower double-digit million euro range, the expansion is to be completed in the first quarter of ...
Tags: Construction, Decoration
US-based establishment Heeren Brothers Produce is recalling around 5,400 cantaloupes as they may have been contaminated with Listeria monocytogenes, according to the US Food and Drug Administration (FDA). The produce associated with the ...
Tags: Heeren Brothers, Cantaloupes
Ensemble Therapeutics has entered into two-part research and development collaboration with Novartis for oral, macrocyclic inflammatory cytokine IL-17 antagonists and additional disease targets. The collaboration will leverage Ensemble's ...
Tags: Ensemble Therapeutics, Novartis
US-based drug development services provider Covance has launched a new service offering to its clients to effectively manage contracts in managed markets. The service offering will help biopharmaceutical and medical device clients to ...
Tags: Covance, drug development services
Stryker Interventional Spine has received 510(k) clearances from the US Food and Drug Administration (FDA) for Venom RF cannula and electrode combination and11g iVAS balloon system. The Venom RF cannula and electrode combination contains ...
The US Food and Drug Administration’s (FDA) Cardiovascular and Renal Drugs Advisory Committee has recommended approval of Bayer’s oral soluble guanylate cyclase (sGC) stimulator, riociguat, in two forms of pulmonary ...
Tags: FDA Advisory Committee
The US Patent and Trademark Office (USPTO) has granted a patent to specialty pharma company AMAG Pharmaceuticals, for its ferumoxytol drug, which is used to heal anemia caused by iron deficiency. The company has been given US Patent No. ...
Adamis Pharmaceuticals has signed an agreement to completely acquire 3M Company's MMM -0.36% Taper Dry Powder Inhaler (DPI) technology. Additionally, the company has entered into an agreement to exclusively license the platform technology ...
Tags: Adamis Pharmaceuticals, Dry Powder