1. Quality control
– Microbiological control (test of sterility) of finished dosage forms and not finished products,
– Chemical and physical analyses.
– Products in immediate packaging
3. Imports from out of European Economic Area in MRA system (incl pharmaceuticals for clinical trials)
– Physical location of delivery,
– Quality control (test of sterility, bacterial endotoxin testing, chemical and physical analysis),
– Release of batches/certification.