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PROXY’s services, whether routine or tailor-made, cover the whole range of QC testing: from compendial testing of pharmaceutical raw materials and excipients to release testing of finished products. In addition, PROXY performs analytical method development and validation thereof.

Design and performance of stability studies, also includes investigation of stability indicating power of key analytical methods. Processes and facilities are supported by our design and validation of cleaning procedures and analytical testing of utility-systems (water, gases). As licensed manufacturer of sterile clinical trial medication we also store and distribute clinical samples to hospitals and other trial sites.
 
Key expertise at PROXY
  • Quality Control testing
  • Quality Assurance services and consultancy
  • Analytical method development and validation
  • Product, process and cleaning validations (chemical and microbiological)
  • Validation of utility-systems (water, gases)
  • Storage and distribution of (bio)pharmaceuticals for clinical trials
  • Stability testing, including storage and stability indicating power investigations
  • EU-import analysis and release
  • Small scale manufacturing of sterile clinical trial medication
  • Residual solvents determination using GC-MS
  • Impurity profiling using UPLC-QTOF-MS
  • Oligonucleotide analysis using UPLC-TQD-MS
  • Monoclonal analysis using CE