| Early-Phase Clinical Studies Worldwide |
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Monitoring ServicesTransCom emphasizes Monitoring quality and efficiency as a paramount in our clinical studies activities. All of our CRAs are fully trained in ICH GCP requirements, standard operating procedures and project specifics to ensure best-in-class quality and speed. We support and supervise our CRAs with senior mentors at the sites and at the office. Our senior personnel have more than 6 years' experience as CRAs and Senior CRAs, to ensure they understand the implications of the monitoring activities at sites. During the study, our project managers review each monitor's activities and visit reports to ensure that the CRAs' performances consistently meet the study's specifications. We perform Initiation, Monitoring, and Close-Out Visits for our strategic partners in many countries. Our flexibility in performing these activities is a significant added value for our partners and clients: we follow either Client or TransCom's SOPs, depending on our client's requirements. For more information about our Monitoring Services, please contact: Sergio Goldfeld |
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