Cleanrooms

qualification / validation / requalification

According with GMP the qualification is an operation which demonstrate the proper function of an equipment and leads in a real way at the expected results. The validation demonstrate that every procedure, process, equipment, material, activity or system leads in a real way at the expected results according with GMP.

Global Pharma Service perform complete project validation, including Design Qualification, Installation Qualification, Operation Qualification, Performance Qualification and Software Qualification for cleanrooms, compressed air and purified water.

All of our measurement equipments used in specific cleanroom testing are calibrated annualy, being accompanied by official certificates.

Find out the types of qualifications/validations/requalifications that we offer and the stages of their development.