We have specialist expertise to

conduct medical device trials

Conducting clinical trials aimed at proving the effectiveness and safety of medical devices is a critical part of the development process for medical device companies and requires significant time, expertise and financial resources to accomplish.

We can assist medical device companies and in vitro diagnostics companies in designing and implementing cost-effective clinical trials of any complexity in full compliance with the principles of good clinical practices and regulatory requirements.


RUSSLAN Clinical Research offers the following services to medical device companies:  preparing study materials, including study protocols, investigator’s brochures, patient information materials, case report forms and any other required documents. Our highly experienced biostatisticians can provide valuable input into the study design.  We offer assistance with regulatory approvals, provide study monitoring and project management, data management, statistical analysis and report writing. We can also conduct sponsor and site audits.