Welcome on Kynetyx HT's Website

Kynetyx HT is Your reliable and full service provider partner in bioequivalence / bioavailability clinical trials. Having a fully integrated organizational structure in one site - a GCP inspected clinical unit and a GLP certified bioanalytical facility - Kynetyx HT assures full control on studies and timely managed bioequivalence results for Sponsors.


26 beds, fully equipped, GCP inspected independent clinical unit with highly trained and experienced clinical investigators assure that your bioequivalence clinical studies are conducted in a well controlled environment on healthy human subjects.

A state-of-the-art, GLP certified bioanalytical facility and the expertize of the analytical staff makes possible to develop, validate bioanalytical methods and analyze biological samples coming from your bioequivalence clinical trials.

Internal Quality Assurance unit with well trained monitors assures that the conduct of your bioequivalence trials is compliant with the GCP & GLP guidelines, internal SOPs, study protocol and EU regulatory requirements.

PK & Statistics, Data Management unit with highly experienced staff designs the best protocol and CRF for your bioequivalence trials and guarantees the compliance of the trial master file with the regulatory agencies requirements.