Training

Aptiance offers a wide variety of training courses. Our experts can teach, troubleshoot and demo a wide variety of projects related to instruments, operation, software, data acquisition, interpretation, and trouble shooting of highly sophisticated innovative instruments such as ultra high pressure liquid chromatography (UHPLC), and LC-MS systems.

Aptiance's experienced instructors have extensive experience in teaching and hands-on-training for LC, LC-MS, LC-MS-TOF, LC-MS-QTOF Ion-trap, LC-MS-MS systems for operation, trouble shooting, detection, software analysis, quantitation, method development, data analysis and profiling and differential analysis techniques. We provide onsite training for professional in the pharmaceutical industry, government agencies/laboratories, and universities worldwide.

Aptiance has expert staff with 30 years experience in the drug development studies which include complex and sophisticated processes such as finding an active molecule from research to pharmacokinetics to clinical trials up to product release and beyond.

Our Consulting/Training Expertise includes:
  • Familiarization and use of state-of-the-art LC, UHPLC, UPLC and LC-MS instruments, software, data analysis and report generating.
  • Theory and techniques for Interpretation of mass spectra.
  • Personalized hand-on-training for LC and LC-MS systems used for drug development, preclinical to clinical applications, sample preparation, method development, identification, characterization, data analysis, quantization, validation, and report printing.
  • Aptiance also provides state of the art cutting edge techniques to various research groups engaged in the study of metabolomics and proteomics.
  • Techniques and tricks for trace level detection of Xenobiotics in bio- and environmental matrices.
  • Trouble shooting and maintenance: ultra high pressure liquid chromatography (UHPLC) and LC-MS.
  • Expert consultation for creating optimized/customized method development for biopharmaceuticals or any active molecular entity.
  • Implementation and validation of LC/MS, LC/MS/MS methods planning and procedure as per FDA guidelines.
  • Alternatives for the enhancement of sensitivity and reproducibility in applications of LC/MS to solving problems in pharmaceutical, biomedical, industrial, and environmental analysis. Specific techniques to improve analytical response and diminish noise and interferences.
  • Stability assays studies planning and procedure
  • Formulation assays for drug substances
  • Interpretation of Mass Spectra training.
  • Identification of Metabolites training.
  • Development, characterization, & implementation of appropriate extraction and purification techniques (e.g., protein precipitation, liquid-liquid extraction and SPE)
  • Biological sample handling and preparation.
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