Cleaning validation is performed to ensure that the equipment cleaning process will consistently reduce the possibility of cross contamination via carryover in a drug manufacturing process. It provides documented evidence that an approved cleaning process will reproducibly remove previous products, by-products of concern or cleaning agent residues that may remain on the equipment to below set limits.

We provide for you:

• Preparation of the cleaning validation documentation:

• Validation plan
• Risk Analysis
• Protocol for cleaning validation
• Final validation report
• Planning & Supervision of Sampling
• Evaluation of the results