Process & Cleaning Validation
Process validation is defined as the collection and evaluation of data, from development through to commercial production.
It establishes scientific evidence that a process is capable of consistently delivering quality product and involves a series of activities taking place over the lifecycle of the product and process.
An essential part of the pharma industry
Process and cleaning validation does not only contribute to the safety and efficacy of medicinal products, it also helps to be compliant with regulations, reduce your production costs and improve the robustness and efficiency of your manufacturing process. It helps to determine the worst case and risks that may arise during the manufacturing of the quality products. In other words, it is an essential part of the pharma industry to get a good, safe, and compliant product to patients.
Our experts can set up, improve and support the qualification and validation of your processes and cleaning.