Flexibility suited for R&D, pilot, and production in a hygienic design, ensuring CIP and SIP capability. Completed with 21 CFR Part 11 conform with SCADA [with WAB-VIEW PRO] system for sterile process. GMP Compliant Equipment Qualification.
Features - Clean-In-Place (CIP) & Sterilization-In-Place (SIP)
- 21 CFR Part 11
- SCADA System availability [with WAB-VIEW PRO]