We use appropriate analytical techniques to ensure that no previously manufactured pharmaceutical products are present from your production equipment. EUROLAB The laboratory quality assurance approach begins from the preparation of an appropriate protocol to the quality of analytical results.
Environmental Monitoring
In accordance with current GMP Annex 1 EUROLAB laboratory provides Environmental Monitoring services for GMP production areas. We specialize in preparing and implementing production site qualification through Environmental Monitoring programs that include air and surface sampling.
We take care of protocol compilation, sampling, testing and reporting. By using molecular biology tools (DNA Microlab), we provide the advantage of fast and accurate microorganism identification. Environmental monitoring services have been implemented in various classified GMP-compliant production areas.
Cleaning Validation
Cleaning validation is important in the pharmaceutical industry. We developed and implemented a microbiological method validation protocol to document method compliance.
We use high performance liquid chromatography (HPLC) to ensure that the routine cleaning you perform on your manufacturing equipment removes all residue of the previously manufactured product. We verify linearity, intermediate sensitivity, recovery and specificity in HPLC test validation. Some of the equipment we tested includes prep and storage tanks, filling nozzles and tools.
EUROLAB, with its highly expert team and internationally accredited laboratories, Cleaning Validation Tests It performs all test, analysis, measurement, evaluation and report generation services completely and reliably.
To get an appointment, to get more detailed information or to request an evaluation, you can ask us to fill in our form and reach you.
