CIP and SIP modules
Clean in Place (CIP) Module
Capacity: - to clean manufacturing vessels from 20litres to 5000litres
CIP is the process used to ensure that process lines, vessels and reactors are free of organic and inorganic contaminants.
Applications:
The CIP module is used in Critical Cleaning Applications in the following manufacturing activities:
- Vaccines
- Injectables
- Serums
- Plasma Fractions
- Suspensions
- Bacteria and Cell Cultures
- Infusion Solutions
Unique Features of the CIP Module:
- Fully automated, microprocessor controlled with touch-screen display
- Integrated validation and automated monitoring system
- Compact system
- User-definable parameters
- Online viewing of process parameters on display
- Once the user configurable cycles are set and validated, a supervisory access code prevents unauthorised changes
- Self diagnosis and error messages
- Printing of process parameters
Sterilise in Place (SIP) Module
The SIP has a microprocessor control system for temperature monitoring throughout the sterilisation cycle
with validation printout facility.
- Operator Interface screens
- Multilevel authorisation password logins
- Fault messages displays
- Fully automated
- Validatable process cycles
Adam Fabriwerk operates a QA system based upon ISO 9001:2000, with documentation compliant with FDA requirements,
including IQ and OQ if required.
All Adam Fabriwerk systems are built according to the following internationally recognised codes:
- ASME Section VIII Div. 1
- ASME BPE 1997; 2000; 2002
- EHEDG Guidlines
Click here to download a pdf brochure.
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