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Articles: Regulatory Issues |
Prior Articles
Saskatchewan pitches Ottawa for reactor
Canadian Healthcare Technology, 08/28/09
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Manufacturing of Biodrugs: Need for Harmonization in Regulatory Standards
BioDrugs, 08/27/09 ARIAD And Its Co-Plaintiffs Announce That the Court of Appeals Granted Their Petition for Rehearing En Banc In the Lilly NF-kB Patent Lawsuit
ARIAD Pharmaceuticals, 08/25/09
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FDA Accepts to File Cell Therapeutics' New Drug Application for Pixantrone
Cell Therapeutics, 08/25/09
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Reference-Standard Material Qualification
Pharmaceutical Technology, 08/24/09
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Chugai Files NDA for a Renal Anemia Agent R744
Chugai Pharmaceutical Co., 08/24/09
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Bristol-Myers Squibb Extends Tender Offer for Medarex, Inc.
Bristol Myers-Squibb Company, 08/21/09
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Mylan Files Lawsuit Against Pittsburgh Post-Gazette
Mylan, 08/20/09 InfoLogix in Financial Trouble
HealthDataManagement, 08/20/09 Gen-Probe Begins U.S. Clinical Study of APTIMA Trichomonas Vaginalis Assay on the TIGRIS System
Gen-Probe, 08/18/09
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BTG Collaborator Onyx Gains Approval to Progress Oncology Compound into Clinical Development
BTG, 08/18/09
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Chugai Files NDA for a Renal Anemia Agent R744
Chugai Pharmaceutical Co., 08/17/09
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Array BioPharma Advances Its Lead MEK Inhibitor into Cancer
Array BioPharma, 08/14/09
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Mylan Pharmaceuticals Receives Final FDA Report and Reaffirms Its 48-Year Exemplary Record of Quality
Mylan, 08/14/09 More than 35,000 cartons of albuterol sulfate stolen
American Pharmacists Association, 08/14/09
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Bristol-Myers Squibb Announces Expiration of Hart-Scott-Rodino Review Period for Acquisition of Medarex, Inc.
Bristol Myers-Squibb Company, 08/13/09
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Wyeth Provides Regulatory Update on Prevnar 13 in the United States
Wyeth, 08/12/09
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Allos Therapeutics Announces FDA Advisory Committee to Review Pralatrexate for the Treatment of Patients with Relapsed or Refractory Peripheral T-cell Lymphoma
Allos Therapeutics, 08/11/09
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Watson Announces Limited Recall Of Fentanyl Transdermal System
Watson Pharmaceuticals, 08/10/09
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PhRMA Statement of Support for Introduction of the Customs
Facilitation and Trade Enforcement Reauthorization Act of 2009
PhRMA, 08/10/09
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