GMP Facilities

  • 200 m2 for CTM production of phase I – III
  • Multi purpose suites with controlled humidity down to 20% RH
  • Inspected and approved by MPA 2003 for CTM production of all non-sterile dosage forms.

GMP Labs and Instrumentation

Compliant with GMP, ICH guidelines and pharmacopoeias
  • Extensive range of fully qualified analytical equipment
  • Comprehensive stability studies expertise
  • Expertise in pharmaceutical analytical method development, validation and QC product testing
  • Equipped with an array of tools and techniques including HPLC, LC/MS/MS, GC, DSC, NGI, Malvern etc.