QUINTA-ANALYTICA

Pharmaceutical ManufacturingPrague, Czech Republic51-200 Employees

Quinta-Analytica is a GCP/GLP/GMP-certified, EMA- and FDA-inspected European CRO delivering fully in-house clinical testing, bioanalytics, pharmaceutical quality control, and analytical R&D/CMC support for small molecules, biologics and biosimilars, generics, and human & veterinary IMPs.

We support pharma and biotech companies globally across the drug development lifecycle from early development through clinical trials, regulatory submission, and market release.

Our main service areas include: 
1) Clinical Testing: With 2 in-house clinical units providing BE/BA/PK studies, with capacity for 60+36 beds.
2) Bioanalytical Testing: GLP/GCP solutions for BE/BA/PK preclinical & clinical studies, small molecules, biologics and biosimilars. PD studies upon request.
3) Pharmaceutical Quality Control: GMP quality control, batch testing, stabilities and HAPIs.
4) Biologics Quality Control: GLP/GMP bioanalysis, CMC, characterizations of peptide & protein IMPs, biosimilars, Cell-based assay.
5) Research & Development: Analytical R&D, impurities, extractables & leachables, degradation, trace studies.
6) Microbiology: GMP sterile & non-sterile testing, microbial/water analyses, endotoxins, antibiotics & vitamins.

Quinta was founded and headquartered in Prague, Czech Republic in 1997 and has been successfully inspected by FDA more than 14 times, including two onsite FDA inspections in 2025.
Quinta is part of the Conscio Group with headquarter in Germany.

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