CPR Pharma 2016

Our state-of-the-art FDA inspected bioanalytical facilities in Australia feature:

  • OECD GLP Recognition with NATA (Australian Government OECD GLP compliance monitoring authority).
  • ISO 17025 Accreditation for Research and Development.
  • LC/MS/MS instruments.
  • Sciex 4000 and 5500 Qtrap.
  • Mesoscale immunogenicity platform.
  • Conventional HPLC (UV-Visible, fluorescence).
  • Low temperature storage with temperature monitoring – multiple unit -80° and -20° C freezer capacity.
  • Generator-backed uninterruptible power.
  • Storage of active facility and study data in fireproof cabinets.
  • Secure access facility.
  • Vendor Assured offsite archive facility with 24 hour security.
  • On and off-site disaster proof storage capabilities.
  • 200 m2 of dedicated laboratory and instrument space.
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