In the pharmaceutical and biotechnological industry qualification is an important part of the GMP compliant manufacturing process. Our goal is to provide you with an ideal and effective support in the accomplishing of your qualification work.

Our services in the field of qualification cover the following main topics:

• Validation Master Plans
• Risk analysis
• Qualification and Validation Plans for all
   project and qualification phases
  (FAT, SAT, DQ, IQ, OQ, PQ, PV)
• Audits of suppliers
• Conduction of qualification work and
  creation of the reports
• Qualification of changes and
  requalificiations