Clinical trial operation services

Pharmaxi is a mid-sized CRO (Contract Research Organization) that operates in Eastern European countries which are appealing places for clinical trials of drugs and medical devices. We support multi-country clinical trials globally through the network of trusted partners. Today our network includes 79 companies from Germany, the Netherlands, France, Israel, South Korea, the United States, etc.

Pharmaxi supports Phase II-IV clinical trials and large-scale non-interventional studies. Our services cover all activities, from study design development to the creation of a final study report. You can delegate selected activities or an entire multi-country clinical trial to Pharmaxi. Centralized project management simplifies trials for our customers. With single contact point (dedicated project manager) and regular reporting we ensure that our cooperation is efficient, requiring minimal effort from the client’s side.

Clinical Trial Management:

Worldwide feasibility studies.
Study start-up: site identification, qualification, and selection.
Contract management.
Regulatory document development and review.
Study document development.
Conducting training for Investigators.
Essential document collection.
Trial Master File set-up and maintenance.
Site monitoring and management (on-site and remotely).
Subject recruitment and retention.
Conducting training for Clinical Research Associates.
Site initiation, monitoring, and close-out.
On-site source data verification.
Medical monitoring.
Sponsor liaison.
Audit preparation.
IRB/EC submissions.
Third-party vendor management.

Our main goal is to provide you with high quality and time-efficient services.

Contact us with your questions or concerns. We offer a free half-hour consultation with a clinical trial expert to discuss your request.