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Found 24,936 articles
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Avedro, Inc. Announces FDA Submission for Corneal Cross-linking
3/9/2012
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Recipharm AB Goes "Green" With Environmental Management
3/9/2012
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Biotechnology Industry Organization (BIO) Hails Senate Passage of PAHPA Reauthorization
3/9/2012
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Drug Information Association Release: FDA Information Days Developed for IT, Regulatory Affairs, and Clinical Research Professionals
3/9/2012
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NCCN Announces New Guidelines for Adolescent and Young Adult (AYA) Oncology
3/9/2012
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Takeda Pharmaceutical Co. Ltd. Hid Actos Adverse Effects From Regulators, Suit Says
3/8/2012
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FDA Rejects Eisai Inc.' Dacogen for AML, Looks at Epilepsy Drug Again
3/8/2012
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Avedro, Inc. Announces FDA Submission for Corneal Cross-linking
3/8/2012
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Aegerion Pharmaceuticals, Inc. Comments on Standard Review Classification for Lomitapide NDA
3/8/2012
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FDA Warns Synthes, Inc. on Device Violations,Threatens Fine
3/7/2012
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USPTO Rejects Butamax’s Self-Described “Foundational” IP Claims in Successful Gevo, Inc. Reexamination Petition
3/7/2012
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Merck & Co., Inc.: FDA Won't OK Its Combo Cholesterol Drug Now
3/6/2012
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Aegerion Pharmaceuticals, Inc. Beats Genzyme Corporation to FDA in Rare-disease Race
3/6/2012
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FDA Accepts Resubmission of Eisai Inc.'s Perampanel New Drug Application
3/6/2012
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Marshall Edwards, Inc. Submits Investigational New Drug Application for Oncology Drug Candidate ME-344
3/6/2012
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TYRX Announces New Medicare ICD-9 Code for the AIGISRx Antibacterial Envelope
3/6/2012
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Australia's Therapeutic Goods Administration is Lax on Device Safety
3/5/2012
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Cappella Medical Devices Ltd Receives Regulatory Approval in India to Market its Proprietary Sideguard® Technology Platform
3/5/2012
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Repligen Corporation Announces Submission of Marketing Authorization Application in EU for SecreFlo™ to Improve Pancreatic Imaging in Patients with Pancreatitis
3/5/2012
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Aegerion Pharmaceuticals, Inc. Submits Marketing Applications for Lomitapide in U.S. and EU
3/5/2012