Amar Q Majjhoo, MD Internal Medicine - Rheumatology Medicare: Accepting Medicare Assignments Practice Location: 29200 Harper Ave, Saint Clair Shores, MI 48081 Phone: 586-777-7577 Fax: 586-777-6841 |
Andrew J Sulich, MD Internal Medicine - Rheumatology Medicare: Accepting Medicare Assignments Practice Location: 29200 Harper Ave, Saint Clair Shores, MI 48081 Phone: 586-777-7577 Fax: 586-777-6841 |
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Soligenix, Inc., a late-stage biopharmaceutical company developing products that address unmet medical needs in the areas of inflammation, oncology and biodefense, announced today that it has been awarded a contract valued at up to $24.7 million inclusive of options by the US Department of Health and Human Service's National Institutes of Health (specifically funded by the National Institute of Allergy and Infectious Diseases or NIAID).
With the 2014 release of its NovoCyte flow cytometer ACEA Biosciences delivered a highly innovative instrument at an extremely competitive price point. In the ensuing three years features such as automated fluidics protocols, a highly flexible and upgradable optical platform, autosampling, direct volumetric cell counting, and the industry leading NovoExpress software have enabled the NovoCyte to quickly gain broad market penetrance.
By affixing nanoscale gold spheres onto a microscopic bead of glass, researchers have created a super-sensor that can detect even single samples of the smallest known viruses. The sensor uses a peculiar behavior of light known as "whispering gallery mode," named after the famous circular gallery in St. Paul's Cathedral in London, where a whisper near the wall can be heard around the gallery.
The Fondation du Centre hospitalier de l'Université de Montréal (CHUM) has received a $1.25 million donation from Pfizer Canada for a patient health education program to be set up at CHUM.
TWi Pharmaceuticals, Inc., today announced that Teh Seng Pharmaceutical Mfg. Co., the manufacturing partner for its generic version of Lidoderm (5% lidocaine patch) located in Taiwan, has completed the cGMP audit and pre-approval inspection by US Food and Drug Administration and been granted "acceptable" status under the FDA's regulatory guidelines.
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