RUSMO-AG, LLC offers the following services:

• Consultations and support study-sites in relations with Sponsors (drug development organizations), CROs (contract research organizations) at the stage of planning, organizing and conducting clinical trials;

• Conducting preliminary work for the conclusion of contracts and (if necessary) quality control of the implementation of CT;

• Providing services to Sponsors and CRO on site selection, conducting feasibility-interview to determine the possibility of participating in planned CT;

• Consultations on forming the optimal study team depending on the planned CT, taking into account the procedures of the CT Protocol and the requirements of the sponsor/CRO;

• Assistance to study sites in enrollment (patient recruiting);

• Home visits service to patients in a complicated epidemiological situation or if the patient does not have the opportunity to visit the study site;

• Consultations of study sites and principal investigators:

- creating, filling in, and storing study documentation;
- planning and organizing the work of medical and diagnostic units used to provide study procedures;
- on the organization of the internal pharmacy for long-term storage of drugs in the framework of study;
- on issues of concluding contracts;
- organization of a centralized archive for storing study documentation (IRC, primary documentation, CRF, etc.);
- on issues of interaction with third-party organizations necessary for conducting CT(vendors). Selection of vendors.