John R Person, MD Dermatology Medicare: Accepting Medicare Assignments Practice Location: 385 Southbridge St, Auburn, MA 01501 Phone: 508-721-1180 Fax: 508-721-9106 |
Dr. Daniel Evan Viders, MD Dermatology Medicare: Accepting Medicare Assignments Practice Location: 207 Southbridge St, Auburn, MA 01501 Phone: 508-832-7118 Fax: 508-832-4758 |
Casey Brown, PA-C Dermatology Medicare: Accepting Medicare Assignments Practice Location: 207 Southbridge St, Auburn, MA 01501 Phone: 508-832-7118 Fax: 508-832-7166 |
News Archive
Sending communications on healthcare benefits through the mail is an important channel in engaging members as they make benefits decisions and as program managers seek to influence member behavior, according to a study on Healthcare Benefit Communications Preferences by Pitney Bowes Management Services, Inc., a wholly owned subsidiary of Pitney Bowes Inc.
SAGE is to launch Foot & Ankle Specialist - European Edition from February 2011. The journal will be an international edition of Foot & Ankle Specialist (FAS), a bimonthly controlled circulation journal launched in 2008 publishing peer-reviewed clinical information for foot and ankle caregivers.
Navidea Biopharmaceuticals, Inc., a biopharmaceutical company focused on precision diagnostic radiopharmaceuticals, announced today that the U.S. Food and Drug Administration (FDA) has accepted the filing of the Company's October 30, 2012 resubmission of its New Drug Application (NDA) for Lymphoseek (Technetium Tc 99m Tilmanocept) Injection.
Nearly 14 million Americans - about one out of every 20 people - have low vision, according to The Centers for Disease Control and Prevention. Eye-care professionals use the term "low vision" to describe significant visual impairment that cannot be corrected with standard glasses, contact lenses, medicine or eye surgery.
The drug was rejected in a 10-6 vote the first time it came before a Food and Drug Administration (FDA) advisory panel, in 2010, due to safety concerns. However when the medication returned for another review in February, the advisory committee gave it near-unanimous approval (20-2). Because the FDA often follows the advisory panel's advice, Qnexa is likely to get FDA approval, probably by mid-April.
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