- 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.