Bio Decontamination Validation
According to Good Manufacturing Practice (GMP) regulations, FDA guidance and USP <1072> manufacturers of finished bio pharmaceutical products must demonstrate that harmful residues or organisms are properly removed during cleaning to predetermined safety levels, thus eliminating contamination of manufacturing equipment.
Vibraclean team has extensive knowledge and field experience.
We support you with robust and accurate validation documentation of our systems.
- SOP development & collaboration
- Selection of biological and chemical indicators
- 3rd party validation services
- Cycle development
- Cleanroom and HVAC solutions for Bio decontamination