Monitoring Force Bucuresti SRL

Your clinical trials need to be conducted with an optimum of quality and reliability, yet speed and budget are just as important. Monitoring Force is a full-service CRO. We design, implement and manage global and local Phase I to IV clinical trials in major therapeutic areas right the first time, saving you time and resources. We offer a comprehensive range of clinical trial management services, with specific centers of excellence in our international organization. We are also experts in putting clinical trials back on track. Monitoring Force is a "right-sized" CRO with flat hierarchies, managed by physicians, where you are treated like a client should be - with respect and responsiveness. The three factors that give us this edge are our highly experienced and qualified people, our thorough planning and management processes and our international presence. Our Services: Concept evaluation Proof of concept consulting Feasibility and market analysis studies Frontloading Clinical Trial Development & Management Clinical Trials Phase I to IV and PMS - design, management and implementation Bioequivalence studies Clinical Trial Crisis Intervention Contract staff services Study protocol, informed consent, CRF (incl. e-CRF) and ancillary documents Study set-up activities Study sites Submissions to authorities and IRB/ECs Investigator/team meetings Study Drug & Supplies Patient recruitment, project management and administration Monitoring Medical support/review Drug safety/SAE reporting Quality control and assurance Statistical Analysis, Data Management, Programming & Medical Writing Biostatistics SAS Programming Data Management EDC (Electronic Data Capture) Medical Writing Compliance FDA Registrations and agent representation IRB/ethics committee & regulatory affairs Specific SOP development for local processes and regulatory compliance Post-study document archiving and retrieval for audits