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GSK and Valeant Announce New U.S. FDA PDUFA Goal Date for Ezogabine
Neuralstem Files FDA Application for First Chronic Spinal Cord Injury Stem Cell Trial
HEMISPHERX SETTLES ALL SECURITIES CLASS ACTIONS Title
PROLOR BIOTECH RECEIVES FDA CLEARANCE FOR A PHASE II TRIAL OF ITS LONG-ACTING HUMAN GROWTH HORMONE IN THE U.S.
FUJIFILM’S FDR D-EVO™ IS NOW AVAILABLE AND SHIPPING
FDA grants Orphan Drug Status for to-BBBs lead product
Aurobindo Pharma receives USFDA approvals for Ampicillin for Injection
Jazz Pharmaceuticals Provides Update on FDA Advisory Committee Meeting For JZP-6 (Sodium Oxybate) in Fibromyalgia
Optimer Pharmaceuticals Fidaxomicin Marketing Authorization Application Accepted for Review by European Medicines Agency
Acceleron Pharma Receives FDA Orphan Designation for ACE-031 for the Treatment of Duchenne Muscular Dystrophy
Gilead Sciences Announces Notification of ANDA Filing for Hepsera(R)
EISAI ANNOUNCES EXTENSION OF FDA REVIEW OF DRUG APPLICATION FOR INVESTIGATIONAL AGENT ERIBULIN MESYLATE
Statement from Eli Lilly and Company Regarding Approval Recommendation from FDA Advisory Committee for Expanding the Pain Indications for Cymbalta(R) to a Broader Pain Population
GlaxoSmithKline and Human Genome Sciences announce FDA priority review designation for Benlysta? (belimumab) as a potential treatment for systemic lupus erythematosus
HUMAN GENOME SCIENCES AND GLAXOSMITHKLINE ANNOUNCE FDA PRIORITY REVIEW DESIGNATION FOR BENLYSTA? (BELIMUMAB) AS A POTENTIAL TREATMENT FOR SYSTEMIC LUPUS ERYTHEMATOSUS
Pronova BioPharma has received Lovaza(TM) Paragraph IV Notice Letter from Teva Pharmaceuticals
ImmunoGen, Inc.Announces Orphan Drug Designation Granted to Lorvotuzumab Mertansine for Treatment of Small-Cell Lung Cancer
Repros Requests Type B Meeting with FDA to Discuss Phase III Protocols for Androxal
CSL Behring Receives FDA Approval to Extend Shelf Life of Hizentra? from 18 Months to 24 Months
FDA Grants Urigen's URG101 Meeting
Endocyte files registration statement with SEC for initial public offering
ArmaGen completes Pre-IND Meeting with FDA for AGT-181
Roche provides update on FDA application for T-DM1
FDA Proposes Withdrawal of Low Blood Pressure Drug
Teleflex Announces Receipt of Approval of All Certificates to Foreign Governments from FDA
EMEA Validates Cell Therapeutics, Inc.'s (CTI) Expanded Pixantrone Pediatric Investigation Plan (PIP)
MESOBLAST ON TRACK FOR PHASE 3 BONE MARROW TRANSPLANT TRIAL FOLLOWING POSITIVE MEETING WITH FDA
Oliver Yeh to Lead NanoInk's Sales Teams in Asia
BioCancell Receives Orphan Drug Approval for BC-819 as Treatment for Pancreatic Cancer
Novartis receives FDA approval of Tekamlo(TM), a single-pill combination of aliskiren and amlodipine to treat high blood pressure
King Pharmaceuticals Launches CYANOKIT? At Fire-Rescue International Expo
Genentech Provides Update on FDA Application for T-DM1
Bristol-Myers Squibb And Pfizer Inc. Evaluate Unmet Need In Patients With Atrial Fibrillation
Data on VIVUS' Qnexa(R) to Be Presented at the European Society of Cardiology Congress
Impax Pharmaceuticals Completes Enrollment in ADVANCE-PD Phase III Trial of IPX066 in Parkinson's Disease