Systec GmbH articles

For the new Systec HX series.
Since 1997, the FDA CFR 21 Part 11 regulations of the American Food and Drug Administration (FDA) have been the international industry-wide standard for the digital documentation of processes in medical technology, medical production and pharmaceuticals. The criteria defined in CFR 21 Part 11 ensure improved efficiency with the automated, paperless and tamper-proof digital processing of process flows and audit trail data. With the “Adv