Pharmaxi is a mid-sized CRO, operating in Ukraine, Poland, and other European countries. These countries are attractive locations for clinical trials.

Pharmaxi positions itself as an effective, client-oriented, flexible, innovative and cost-attractive company.

The main focus of Pharmaxi is the conduction of phase II-IV clinical trials and late-phase large-scale non-interventional studies. Services embrace all types of activities, from study design negotiation to the final study report creation. If some specific tasks are not covered by in-house facilities, (e.g. drug depot, logistics, insurance), we subcontract them to trusted and fully-vetted local vendors.

In rare cases, we develop unique services (including SOPs and working instructions) on demand. So, feel free to contact us to make sure that your clinical trial services are not only well coordinated and conform to international standards, but also exceed your quality and budget expectations.


Site Management

Pharmaxi identifies the best investigational sites for the study and provides management and necessary support. Feasibility takes into account the following: therapeutic area, requirements for investigators and sites, technical equipment and other important elements. Qualification Visits, SDV, and Closeout Visits are carried out on-site by qualified personnel. Training of investigators, data collection progress and data cleaning are executed remotely with EDC system OnlineCRF, which makes the project transparent and well-driven. CRAs and CTLs can control patient enrollment, the number of completed/incomplete CRFs, the number of CRF editing and the reason for the change. Each type of user can oversee various project indicators. The Project Manager can view the overall study progress and CRA activity. CRAs have access to the activity of subordinate investigators only.

Scope of services

We are focusing on clinical trials management and we love to conduct clinical trials from the study design development up to the final study report and TMF provision. At the same time, we deliver selected services (medical writing, site management, data management, on-site monitoring, etc.) per the client’s request. Trying to provide full service from one hand, we assemble more than 30 companies covering multiple countries and we conduct multi-country studies together. We collaborate with multiple experts in different areas and this gives us unprecedented coverage and the ability to provide a wide range of services.

Clinical Trial Management

The Clinical operation and administrative team takes care of the local Ethics and Regulatory Submissions, provides support in Contracts Management, maintains the Trial Master File and essential documentation during the project.

Medical Writing

We can assist you with the preparation of all documents (e.g. Standard Operating Procedures, Clinical Study or Pharmacovigilance Reports, Study Protocol, Investigator Brochure, Informed Consent Form or Case Report Form).
"We’ve been working with Pharmaxi since 2014 in frame of epidemiological multicentre study in Ukraine and the Baltic countries in the field of hepatitis C. We are satisfied with the work of the team that demonstrates the high level of professionalism and quality in the design and management of clinical databases."
Galyna Bryn, CIS Medical Directo
"Pharmaxi LLC maintains the high professional level of personnel and clear processes aimed at goals achievement. We recognize Pharmaxi LLC as a trustworthy partner with a responsible attitude to their obligations and consider them to be a team of experts in the profile activity. We recommend Pharmaxi LLC as a reliable and stable business partner."
Alla Gontar, Medical Head
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