The CTI Difference: Cleaning Validation Services
CTI understands the importance and the complexities of building a sound cleaning validation program. Cleaning procedures and corresponding cleaning validation approaches vary with each product. By evaluating each project’s many variables and identifying the critical few, we minimize the sampling and testing required, to provide the best value validation solution.
CTI’s subject matter expertise derived from diverse project experience in the pharmaceutical and biopharmaceutical industries can help you develop cleaning processes and cleaning validation strategies consistent with current best practices. Our objective is to design a risk-based and science-based cleaning validation strategy that eliminates contamination risks that may contribute to poor product quality. By taking the time to understand your cleaning processes and each of your product’s solubility, toxicity, biological and chemical properties, and by studying your equipment’s design and product contact surfaces, CTI helps you determine the worst-case cleaning scenario to improve effectiveness and efficiency of your validation program.
In the end, it’s all about the patients you serve; patients who expect and deserve a safe product free of undesired biological and chemical carryover. CTI can help you manage and execute your cleaning validation program and help you deliver the highest quality products. Let us know how we can help support your organization.