CLEANING VALIDATION SUPPORT
Establish reliable cleaning procedures – and prevent your product from being contaminated.
In our experience, pharmaceutical companies often struggle with cross-contamination control and cleaning validation. Studies such as the Annual GMP Inspection Deficiencies Report show that they’re among the most observed critical and major deficits during inspections.
If different pharmaceutical products are manufactured in shared facilities, there’s always a risk of cross-contamination due to residues of pharmaceutical ingredients, by-products, or detergents. To ensure the quality and safety of your product doesn’t get compromised, the cleaning process is essential.
PDE and cross-contamination risk assessment
The first step to reduce danger for people using your product is to determine how many residues of a certain substance could still be in the used equipment without causing any harm.
The right strategy and measures tailored to you
After determining limits and risks, we ensure that any residues in facilities and equipment are removed down to acceptable levels through cleaning. We assist you in to detailing the process: cleaning validation serves as a documented guarantee that your cleaning procedures are effective and can be performed reliably and repeatedly.
In order to achieve this, our team of toxicology experts takes care of:
