At Validation Science, we hope to become your source for analytical method development, method validation, and related topics and services as they relate to pharmaceutical drug discovery and development. We are globally recognized leaders in pharmaceutical analytical development and regulatory compliance, having consulted for private industry, trade organizations, and lectured around the world.

Our technical expertise includes:

  • GMP, CRO/CMO facilitation and management.
  • Separation and identification of both small molecule synthetic and biologic pharmaceutical compounds using technology including: High Performance Liquid Chromatography (HPLC)- Capillary to Preparative Scale, Ultra High Performance Liquid Chromatography (UHPLC), Capillary Electrophoresis (CE) and Gas Chromatography (GC);
  • Mass Spectroscopy (MS and MS/MS), Ultraviolet (UV) and Infrared (IR) spectroscopy
  • Dissolution, Karl Fischer (KF), Chiral (enantiomer) Assays

Web Casts:

  • Web Casts from Validation Science are available on a variety of topics, and can be custom-tailored to your needs.
    For a complete list of topics, or to request your own,
    contact us.
  • LC/GC Magazine also offers web casts on a variety of topics:
    Click here for more info

Recent Presentations

  • Development and Validation of HPLC-Corona CAD/UV Stability Indicating Methods.
    For more info
    contact us
  • Migrating Traditional Methods to Sub-two micron Particles.
    For more info
    contact us
  • Design and Implementation of a Forced Degradation/Chemical Stress Study Using New LC Column Technology.
    For more info
    contact us
  • Chromatographic Analysis of Bisphenol A: A Comparative Study.
    For more info
    contact us

News and Announcements

  • Recently Published: "Handbook of Analytical Validation"
    Click here for more info.
  • Recently Published: Chapter 12, Method Validation, in: "Introduction to Modern Liquid Chromatography".
    Click here for more info.
  • Just published: “Contemporary LC Systems for Method Development,” Chapter 6 in HPLC Method Development for Pharmaceuticals, Edited by Satinder Ahuja.
    Click here for more info.

Interested in becoming a Sponsor or Partner?

Contact us and we can provide you with additional information.

    RioDesign Ltd.
homepage contact us terms privacy policy