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Recent related articles ( announces fda):

Sorin Group Announces European Market Release And First Implant Of New-Generation Cardiac Resynchronization Therapy Defibrillator
Sorin Group, (MIL:SRN), a global company and a leader in the treatment of cardiovascular diseases, announced today the commercial market release and first implant of its new-generation PARADYM? CRT 8750 cardiac resynchronization therapy defibrillator (CRT-D). Together with the new SITUS? BW 28D left ventricle pacing lead and lead
Sorin Group Announces European Market Release And First Implant Of New-Generation Cardiac Resynchronization Therapy Defibrillator...

Arthritis Advisory Committee Recommends FDA Approval of Febuxostat for the Treatment of Hyperuricemia in Patients With Gout
Takeda Pharmaceutical Company Limited and its wholly-owned subsidiary, Takeda Global Research & Development Center, Inc., U.S., announced today that the Arthritis Advisory Committee of the U.S. Food and Drug Administration (FDA) recommended that the FDA approve febuxostat for the treatment of hyperuricemia in patients with gout.
Arthritis Advisory Committee Recommends FDA Approval of Febuxostat for the Treatment of Hyperuricemia in Patients With Gout...

Antiinfluenza Medication Kits Need Work, FDA Advisers Conclude
A proposal to let Americans stockpile prescription antiviral medication in their homes in advance of an influenza pandemic drew a lukewarm response from a panel of experts convened by FDA.
Antiinfluenza Medication Kits Need Work, FDA Advisers Conclude...

[news] fda opens office in china to regulate safety of exported drugs

[news] fda opens office in china to regulate safety of exported drugs...

Medarex Announces Initiation of Phase 1b Clinical Development Program with MDX-1106 for the Treatment of Cancer
Medarex, Inc. (NASDAQ: MEDX) today announced it has initiated a Phase 1b clinical trial for MDX-1106 (ONO-4538: development code of Ono Pharmaceutical Co., Ltd.), a fully human anti-PD-1 antibody for the treatment of cancer.
Medarex Announces Initiation of Phase 1b Clinical Development Program with MDX-1106 for the Treatment of Cancer...

FDA Approves Tapentadol As Pain Reliever
Johnson & Johnson Pharmaceutical Research and Development LLC announced today that FDA approved the marketing of tapentadol immediate-release tablets for the relief of moderate to severe acute pain in adults.
FDA Approves Tapentadol As Pain Reliever...

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