We use tests for pharmaceutical products, also known as preservation efficacy testing (PET), to evaluate the ability of your pharmaceutical products to protect against microbial contamination.
Why is trial testing important?
We conduct tests to demonstrate the ability to protect against microbial contamination that may occur under reasonably predictable storage and handling conditions.
Ideally, pharmaceutical products should be tested at development stages.
Our accreditation scope
We have received EU Good Manufacturing Practice (GMP) certification by the Greek National Pharmaceutical Organization (EOF) for microbiological testing (without sterility) of human and veterinary medicinal products in various dosage forms.
Which challenge test protocol we use
EP reference standard
European Pharmacopoeia (EP) reference standards involve challenging final container preparation wherever possible. Uses a prescription vaccine of suitable microorganisms (Pseudomonas aeruginosa, Staphylococcus aureus, E. coli, Candida albicans, Aspergilus brasiliensis).
Scanning is done as follows:
Conclusions
Results can be obtained within 35 days.
The protective properties of the preparation are suitably sufficient in the case of a significant decrease or no increase in the number of microorganisms in the inoculated preparation, the prescribed temperatures and time.
During the scanning process, you get real-time preliminary reports on intermediate readings. In some cases, we offer a 24-hour courier service.
Minimum sample amount
100 gram
EUROLAB, with its highly expert team and internationally accredited laboratories, Trial Test 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.
