Clinical Facilities
Bioanalytical Laboratory
Who we are and what we do:
PHARMBIOTEST POLAND is a privately owned, full-service CRO (Contract Research Organization) headquartered in Grudziądz, Poland
Video about the center
For more than 7 years, PHARMBIOTEST offers clinical trial management and conducting service from small pilot studies to large multicenter international clinical trials for all phases (1-4), including bioequivalence studies in accordance with EU Directives, internationally accepted guidelines and standards, like ICH-GCP or GLP and national laws. PHARMBIOTEST is committed to high quality, dedicated customer service, integrity and operational excellence.
If you have any questions regarding the planning and conduct of a clinical study, contact our team at
call +38 (050) 367 62 33 or fill out the feedback form.
What do you get by ordering a study from us
Full package of services
Our center provides bioequivalence research services, including the clinical, bioanalytical and statistical stages, and we also make a package of documents: from the development of a study protocol to the preparation of a study report.
Quality
Each study is conducted in accordance with Good Clinical Practice (GCP) and Good Laboratory Practice (GLP). The Quality assurance unit (QAU) proceeds according to internal regulations and monitors the compliance of each step of study.
True cost
All stages of the study are carried out by one company, which significantly reduces logistics costs.
News
October 9 - 12, 2018 | Ukraine
The Quality Director of MTZ Clinical Research conducts workshops on the principles of good clinical practice (GCP) accredited by Transcelerate at a partner Research Center in Ukraine.
October 2018
In October 2018, our company passed the audit to confirm compliance of clinical research practice with the appropriate ICH GCP E6 (R2) requirements and Ethical Principles.
