Wrap & Comply

It is not always necessary to replace your legacy systems to comply with current regulations…

The “Wrap & Comply” concept looks at working with your current system components to minimize your validation effort. Maximizing the re-use of hardware and software will enable you to “Wrap” your legacy system in a compliant architecture in order for the GxP system to “Comply” with regulatory requirements including the FDA’s 21 CFR Part 11.

Save time and money…

Re-use existing hardware
Re-use existing software
Minimize SOPs
Improve plant efficiency and quality
Faster time to market
Reduce validation

Let us help you identify the non-compliant systems and take the necessary remediation action to validate them:

Gap analysis – Identify computer system validation gaps
Coverage Assessment – Determine which GxP rules must be satisfied
Risk Assessment – Determine and prioritize potential compliance actions
Mitigation/Remediation Plan – Formulate a corrective action plan addressing the deficiencies following the rule: “Maintain as much of the existing hardware and software as possible”
Implementation – Implement corrective actions