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Quality Compliance Laboratories
Raw Material (RM), Active Pharmaceutical Ingredients (API's), Pharmaceutical Intermediates, Excipients, In-process Testing , Finished Product Release , Trace Contamination ID , Organic Volatile Impurity (OVI) , Stability , Technology Transfer , Container Closure Testing , Assay (HPLC, GC, UV-Vis) , Dissolution esting (UV & HPLC) , Disintegration , FTIR , TLC , Cleaning Validations , Content Uniformity , Metal Analysis Heavy Metals , Water Testing , Total Organic Carbon (TOC) , Conductivity , Karl Fischer/LOD , Moisture Analysis , Residual Solvents , Organic Volatiles , Optical Rotation , Drug stability testing for liquid/injectables , Impurities , Melting Point , Viscosity , Osmolality , Compendial Tests , Solubility , pH and titrations , Partition coefficient , pKa measurements , Stability Protocol Design , Long Term Stability, Accelerated and Intermediate Studies, Drug Substance Stability Testing, Stability testing for IND, NDA, ANDA , Commercial/Marketed Products, Formulation Evaluation Stability Testing, Forced Degradation Studies, Photostability and Temperature Cycling, Potency , Dissolution , Related Compounds/Impurities , Moisture , Residual Solvents , Physical-Chemical Tests , Cleaning Assessment , Drug Master File (DMF) Updates , Filter Evaluation / Method Precision, Limit of Detection (LOD) , Limit of Quantitation (LOQ), Accuracy / Precision, Recovery Studies, Linearity , Specificity, Forced Degradation, Range / Robustness, Solution Stability, Analytical Method Development and Validation, Technology Transfer, Method Feasibility, Process Validation, Shelf-life and Other Stability Analyses, Long-Term Stability Testing, Accelerated Stability Testing, Forced Degradation Studies, Quality Compliance Consulting Services
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