Process Control & Validation

Eurofins Biopharma Product Testing in Italy provides full GMP-testing for the qualification or monitoring of your facility. We provide support for setting up protocols and /or sampling programs and identification of the risks inherent of each type of qualification / validation / monitoring.

Our services can be customized according to Client's specific necessity. We can performing testing on samples collected at Client's site or directly at Client's facility. Samples transportation (in ambient conditions or refrigerated) can also be performed as well as transport validation, necessary to ensure proper compliance with regulatory requirements.

We can also perform documentation validation and qualification by defining the most appropriate sampling plan. All our validation services are based on a risk analysis approach.

With over 20 years of experience on process control & validation we provide the most accurate panel of services through highly trained analysts, technical experts, and sampling specialists to ensure accurate and timely results. All our validation services are based on a risk analysis approach.

We have a deep understanding of the regulatory and legislative pressure that all companies face. All test are performed according principal pharmacopeia (EP, USP, JP, ChP) and ISO Guidelines.

• Environmental monitoring
• Water and steam testing
• Gas testing
• Media-Fill sterility and Growth promotion
• Bioindicators testing
• Sterile dressing validation
• Validations of cleaning processes