VISIOTT manufactures serialization machines proper for the pharmaceutical industry needs. These machines can carry out high-speed and sustainable serialization and aggregation processes. Besides, these processes comply with the pharma serialization regulations of EU-FMD, DSCSA, Russia, Turkey, and other countries.
Our serialization machines can work with frequently used packages (cartons, bottles, Tetra Paks, vials, ampules, and blisters) in the pharmaceutical industry. However, we can easily customize our machines for different packaging types.
We design our serialization machines to be operated fully integrated or independent with the pharmaceutical seconder packaging (drug) production line. In addition, we follow hygiene, material, and safety rules determined by GMP guidelines in our designs.
We constantly develop the software we use in our serialization machines. Therefore, we can configure the line manager (Level 2) software developed by VISIOTT engineers according to user needs. Also, we take into account GAMP5 and 21 CFR PART 11 requirements when developing our line-level software.