• Pharma/Biotech lab

    –Help integrate UHPLC with advice on the purchase, set up, method translation and issue avoidance

    –Expedite HPLC method development for assays and impurity analysis with a 3-pronged template approach, a universal generic gradient methodology, and mass spectrometry

    –Design of stability studies to improve data quality to minimize issues
     

  • Regulatory filing and CMC

    –Streamline CMC quality data for IND/NDA filings with IQ Consortium guidelines

    –CMC data review and help resolve analytical issues

    –Training on the entire drug development process and drug quality fundamentals to increase understanding of this multidisciplinary and complex process
     

  • HPLC instrument and column manufacturers

    –Devise and implement marketing strategies for pharma/biotech customers for instruments, data/applications systems, and columns
     

WHY US?

EXPERTISE, SPECIALTIES AND STRENGTHS