If you are a romanian citizen please visit our page on the following link: voluntariat

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 clinical trials is compliant with the GCP & GLP guidelines, internal SOPs, EU regulatory requirements.	PK & Statistics, Data Management unit with highly experienced staff designs the best protocol and CRF for your bio-equivalence trials and guarantees the compliance of the trial master file with the regulatory agencies requirements.