Our strength is in our experience

at every stage of a clinical trial

At any stage of a clinical trial, from protocol planning and design through clinical conduct to data management and medical writing, our clients can be assured of our high performance standards and expertise.

In the field of late stage clinical development (Phase IIb – IV), our services include:

• Feasibility studies
• Clinical trial planning and design
• CRF design and printing
• Selection of efficient clinical trial sites
• Regulatory affairs
• Translation of study documentation
• Training in GCP
• Investigator meetings
• Site monitoring from pre-study to close-out visits
• Project management
• Management of trial supplies, including import/export licences
• Pharmacovigilance
• Quality Control and Assurance
• Data management and biostatistics
• Medical and scientific writing
• Patient enrolment and retention

Early stage clinical development (Phase I-IIa):

In a partnership with two leading early stage clinical trial units based in Russia and Ukraine, RUSSLAN can offer:-

• Safety and tolerability studies
• First in man studies
• Bioavailability and bioequivalence studies
• PK/PD studies
• Drug-drug and drug-food interaction studies

Our Phase I/IIa units are well equipped and staffed with experienced medical, pharmacology and laboratory staff, and are attached to large tertiary hospitals with full intensive medical facilities.