Site Management Organization (SMO)
Bosker Medico services has a comprehensive understanding of the entire research process and can effectively manage each stage of study including site evaluation, site initiation, site management, and site closeout. Our experience allows us to quickly address any issues, make necessary adjustments, and maintain efficient communication with all stakeholders involved, which leads to the overall success and smooth execution of clinical trials or research projects. Clients and collaborators can have confidence in our ability to handle the studies effectively and ensure timely progress and completion.
We provide qualified and pre-screened principal investigators for clinical trials, which help us in providing access to a large patient study population that leads to enhancement in the recruitment process for these trials. By streamlining the process of connecting investigators with trials and facilitating ongoing communication, we contribute to the efficiency and effectiveness of clinical research.
We have experienced and receptive team with the knowledge of all phases of clinical trials and regulatory guidelines (ICH-GCP, FDA, ICMR, CT Rule 2019 and Schedule Y). Hence, we provide strict compliance with study protocols and timelines.
This, in turn, can lead to more timely and accurate data collection, analysis, and ultimately, better outcomes for patients involved in the trials.