CQV Cleaning Validation

Prevent Contamination and Protect Your Organization with Cleaning Validation Services from Transcat

Cleaning validation is a critical step in preventing cross-contamination – and verifying the efficacy of your cross-contamination strategy. Relying on Transcat to conduct an initial qualification of your manufacturing process and equipment is an ideal starting point.

CQV Cleaning ValidationCQV Cleaning Validation

The Right Cleaning Support for Your Industry and Processes

In pharmaceutical and biomedical applications, cross-contamination between products can compromise patient safety, halt production, cause batch failures, and result in FDA rejection – which can lead to costly fines.  

Components used in the pharmaceutical process, chemical deposits, and microbes are particularly susceptible to cross-contamination, making regularly scheduled cleaning validation essential. 

Our CQV Cleaning Validation Services team will manage your cleaning validation and effectively 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 Operating Procedures for Better Reporting & Validation

Our team will ensure that 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, as well as the criteria for acceptance and the circumstances under which re-validation will be necessary; documented protocols are created for inspecting each piece of equipment; and reporting is prepared to determine validity of the cleaning process.  

Discover how Transcat can customize a solution for your unique cleaning validation needs.