PHARMBIOTEST provides a full range of services for pharmacokinetic and bioequivalence studies
All procedures: study design planning, medical writing of study protocol, CRF / source data form design and other required documents, preparation of documents for regulatory submissions, ssubject recruitment, clinical conduct of the study, project and site management, analysis of PK samples, data management and statistical analysis, reporting of study results and archiving of all trial-related data are conducted in accordance with GCP/GLP guidelines.
Let us guide your study!
WHAT WE DO
PHARMBIOTEST offers a full services of bioequivalence/pharmacokinetic studies.
Clinical Trial Documents Development
PHARMBIOTEST has experience in clinical trials and provides document development services for phase I-IV clinical trials.
PHARMBIOTEST bioanalytical laboratory provides services of quantifying ultra low concentrations of small and medium-sized organic molecules in biological samples in the course of preclinical trials.
PHARMBIOTEST provides statistical support of clinical trials (pharmacokinetic studies and bioequivalence studies, dose-proportionality, efficacy, tolerability, safety, etc.)