Cleaning Validation Services
Critical Cleaning Validation Solutions
In pharmaceutical and biomedical applications, cross-contamination can compromise patient safety, halt production, cause batch failures, and result in FDA rejection – which can lead to costly fines.
Cleaning validation is critical to preventing cross-contamination, and essential to verifying the efficacy of your cross-contamination strategy. Components used in the pharmaceutical process, chemical deposits, and microbes are particularly susceptible to cross-contamination, making regularly scheduled cleaning validation essential.
Get the Best Cleaning Support for Your Needs
Clients trust Transcat to perform qualifications of their manufacturing process and equipment in order to customize the right cleaning solution. Transcat’s CQV Cleaning Validation Services team not only manages cleaning validation; we will equip you to prevent contamination by:
- Clearly defining products
- API Solubility Matrix / Equipment Train
- Establishing acceptable limits
- Providing testing support
- Performing post-implementation reporting
Streamlined Solution that Enable Better Reporting & Validation
Our team will ensure:
- Standard operating procedures (SOPs) are developed for the cleaning processes of utilized equipment
- Written procedures are created to specify the responsibilities for performing and approving the validation study
- Written procedures are created identifying the criteria for acceptance and the circumstances under which re-validation will be necessary
- Documented protocols are created for inspecting each piece of equipment
- Reporting is prepared to determine validity of the cleaning process
Discover how Transcat can customize a solution for your unique cleaning validation needs.
Request a quote using the form below. Questions? Connect with our team today.
