There is a well-defined and independent WHO-GMP-compliant Quality Control unit with the following salient features:

  • A written Quality Policy.
  • Independent Quality Control Head.
  • Complete documentation system with written procedures for each activity.
  • Well-equipped laboratories with certified and calibrated instruments.
  • Qualified & Experienced Staff / Analysts. Established in 1989 as Joint Venture with Vineland Labs, U.S.A.
  • Activities of the Quality Control Department:
    1. Physico-Chemical Testing

Testing of

      • Diluents, RM & PM.
      • Samples of water – Potable water D.M & WFI.
      • Moisture content in lyophilized vaccines.
      • Residual formaldehyde -Inactivated vaccines.
    1. Bio-Analytical Testing
      • Microbiological and Biological Analysis of Vaccines (DS & DP).
      • Stability Testing of Vaccines (DS & DP) and Diluents.
    2. Microbiological Testing
      • Media Preparation.
      • Environmental Monitoring.
      • Sterility testing of vaccines (DS & DP), diluents and water samples.
    3. biological Testing
      • Serological/ Potency testing of vaccine samples.
      • QC testing in Embryonated eggs and Tissue-culture.
      • Safety and Innocuity tests.