Cleaning Validation
We specialize in Cleaning Validation (CV) programs designed to ensure patient safety, product quality, and regulatory compliance. Our team provides proven strategies for cleaning validation/verification, cycle development, and lifecycle maintenance.
Areas of Expertise
- Cleaning validation master plans
- Risk-based cleaning assessments
- Maximum allowable carryover calculations and acceptance criteria
- Relative cleanability and worst-case assessments
- Residue limit calculations and acceptance criteria
- Swab and rinse sampling strategies
- Visual inspection qualification
- Re-validation and periodic verification programs
Best Practices
- CIP and SIP cycle development
- Recovery studies and clearance verification
- Proactive troubleshooting and deviation resolution
- Robust documentation for audit readiness
Work with Forza Pharma Consulting to design cleaning validation programs that safeguard compliance and product integrity.
