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Method Development, Method Validation, Chemical Testing Lab,
www.validationinc.com - 2009-02-08
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PharmSep: LCGC's Symposium for Separation Scientists in Pharma and Biopharm is brought to you by LCGC North America, the leading technical magazine for ...
LCGC Conference  LCGC Event LCGC North America LCGC Symposium Method Qualification
www.lcgcevent.com - 2009-02-06
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Ventura Associates is a company with expertise in reviewing and remediating cGMPs, Validation requirements that the Pharmaceutical Industry is expected to ...
pharmaceutical audits ventura associates
www.ventura-assoc.com - 2009-02-11
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3rd Workshop on Recent Issues in Regulated Bioanalysis April 16-17, 2009 Short Courses April 15, 2009 Montreal, Canada _______________ CVG/Therapeutic Products ...
Instrument Qualification Validation Group
www.cvg.ca - 2009-02-10
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NDA Analytics - your first choice for outsourcing pharmaceutical analysis.
biopharmaceutical analysis compound characterisation immunological tests product characterisation QC release
www.nda-analytics.com - 2009-02-06
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Robertson Microlit Laboratories...Quantitative elemental microanalysis and trace analysis...Structure determination of pharmaceuticals and chemicals.
CHNSX Dr. Franz Scheidl Log D robertson microlit sulfur chlorine bromine
www.robertson-microlit.com - 2009-02-04
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Providing creative chemical and technical solutions to meet your particular needs focusing on inorganic product development and analysis.
Analysis. Consultant BET Surface Area BET SA Inorganic Product Development Kathy Thrush LECO Carbon Analysis New Product Characterization Particular Solutions Samples Fusion X-Ray Fluorescence XRF
www.particularsolutions.com - 2009-02-13
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RegiLabs is a leading independent contract laboratory, internationally renowned for top-quality chemical and microbiological analysis, support and advice.
www.regilabs.com - 2009-02-06
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FDA Consultants/Regulatory Advisors to the Pharmaceutical, Medical Device, and Food Industries. Call Phoenix Regulatory Associates, Ltd. for insightful guidance ...
FDA regulatory consultants FDA surveillance form 483 responses Frank Fazzari GCP vendor audits Juice HAACP post market reports preclinical toxicity trials
www.phoenixrising.com - 2009-02-14
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MJ Pharm Consulting - Pharmaceutical and Analytical Sciences.
analytical troubleshooting deficiency letters responses drug product specification drug product testing drug substance specification drug substance testing in-vitro bioequivalence method validation protocol method validation report post-approval change pre-formulation studies stability protocol
www.mjpharm.com - 2009-02-09
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