Clinical trials of drugs and medical devices

Monipol International is a Contract Research Organization and on behalf of pharmaceutical organizations, NGOs, academic sponsors and other CROs flexibly adjusts to the needs of each of our Sponsors. We conduct international clinical trials of medicinal products and medical devices in all four phases required for marketing authorisation in the pharmaceutical market. We also offer conduct of GCP audits of phase I-IV clinical trial study sites. Monipol International consists of the Polish company Monipol International Sp. z o.o. and the German Monipol International GmbH.

Our cooperation with other European CROs that are members of the international organization Across Alliance enables us to provide a comprehensive range of services to meet the individual needs of our Sponsors. We focus on clinical trials conduct in Poland and in German-speaking countries, but in cooperation with European partners we also conduct international multi-centre trials throughout Europe. We are also a member of the Polish Association for Employers of Contract Research Organization (PolCRO).

Clinical trials

Under the name Monipol International, two companies operate in Poland and in Germany, which together offer a wide range of CRO services. Gained experience and facilities enable us to conduct phase I-IV clinical trials throughout Europe. We follow international standards and GCP principles.

Audits

The quality control of study sites according to the international guidelines is among services provided by Monipol International. Our GCP auditor has 20 years of experience of working in clinical trials and has conducted over 50 GCP audits in Poland, Slovakia, the Czech Republic, Hungary, Germany, Ukraine and Russia.