harmaceutical Facility Cleaning - FDA cGMP Compliant for Patient Safety
What Pharmaceutical Facility Managers Tell Us They Need
Patient safety depends on cleanliness
Pharmaceutical contamination can harm patients and trigger massive recalls. Our cleaning procedures follow FDA cGMP requirements and prevent cross-contamination that could affect drug safety and patient health.
FDA inspections are comprehensive
FDA facility inspections examine cleaning procedures, documentation, and validation records. Our procedures meet FDA expectations and provide the detailed documentation required for regulatory compliance.
Cross-contamination must be prevented
Different drugs manufactured in the same facility require validated cleaning to prevent cross-contamination. We use validated procedures, dedicated equipment, and appropriate cleaning agents that ensure complete product removal.
Sterile areas require special protocols
Aseptic processing areas demand sterile cleaning procedures and specialized techniques. Our technicians understand sterile processing, use appropriate materials, and maintain sterile conditions during cleaning operations.
Validation documentation is extensive
Pharmaceutical cleaning requires validated procedures, cleaning verification, and detailed documentation. Our CleanAudit360 system provides the documentation needed for validation and FDA compliance.
