Skip to content

www.pharmbiotest.com use cookies to help us improve the website and your experience using it. You may delete and block all cookies from this site at any time, details of which can be found in our cookie policy. However please note this may result in parts of the site no longer working correctly. If you continue without changing your settings we will assume you are happy to receive all cookies on this site.

Your Partner for Clinical Trial Management and Research

R&D and Early Phase Studies

folder

Clinical Facilities

microscope

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

For over a decade, Pharmbiotest Poland has been a trusted partner in clinical research and bioanalytical services, providing high-quality solutions to the pharmaceutical and biotechnology industries. As a GLP/GCP-certified CRO, we support the full lifecycle of clinical trials and pharmaceutical development, ensuring compliance with international regulatory standards.

Our expertise extends beyond clinical trials, encompassing the research and development of generic and hybrid medicines, helping bring safe and effective treatments to market. With a dedicated team of specialists and state-of-the-art facilities, we are committed to delivering accurate, reliable, and timely research outcomes that meet the evolving needs of our partners.

At Pharmbiotest Poland, we prioritize scientific excellence, operational integrity, and a client-focused approach to support innovation in drug development.

If you have questions about our services, you can contact us at:

.

call +48 736 335 818, or fill out the feedback form

Contact us
Name *
E-mail *
Message
Please indicate that you have read and agree to the Privacy Policy

What You Get by Ordering a Study from Us

case-01

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.

case-02

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.

case1-03

True cost

All stages of the study are carried out by one company, which significantly reduces logistics costs.

>
Bioanalytical methods
MS-systems