QUINTA-ANALYTICA s.r.o. is a Contract Research Organization (CRO) which offers a comprehensive range of services in all described activities.
We have an excellent group of investigators, medical staff (including physicians and nursers), bioanalytics, biostatistics and study coordinators. This represents an experienced team of more than 30 specialists guaranteeing fast, exact, flexible and competitive service in price of all required activities.
QUINTA-ANALYTICA s.r.o. provides all these complete services in one package or in accordance to the sponsor’s requirements it is also possible to offer independent clinical, bioanalytical or pharmacokinetic and statistic evaluation.
For our in-house studies we accommodate volunteers in our modern thirty-six bed Clinical Centre which enables all necessary care and comfort. We offer integrated services, from the study design and protocol, to study conducting, up to final report writing.
Our Bioanalytical department, in addition to our Clinical Centre also co-operates with other clinics and test facilities across the globe. This department has successfully passed through FDA inspection.
All activities are processed in close co-operation with the sponsor and they are performed in systems of Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) under the supervision of our Quality Assurance Unit (QA).
Our services:
- Preclinical studies (toxicokinetics); we ensure complex service, and samples are analyzed in our own laboratories
- Bioequivalence studies /I.-IIa phase
- Pharmacokinetic and pharmacodynamic studies on special subject populations
- II.-IV phase clinical trials
- Development and a validations of bioanalytical methods in different biological matrices
- Bioanalyses
- Evaluation of pharmacokinetic and statistical data
- Blood level analyses of pharmaceuticals
- Packaging, blinding and release of Investigational Products under Good Manufacturing Practice (GMP)
- Archiving of all documentation concerning the study/trial
Company
