Clinical trial management and monitoring must adapt with the new complexities which we are facing in modern clinical trials.  By implementing quality risk management systems such as Risk Mitigation Plans and protocol evaluations, Triumpharma collaborates to maintain focus and flexibility with specific attention to the study objective, design, complexity, size, and endpoints. Striking the delicate balance between centralized and on-site monitoring needs, as well as careful consideration of targeted source data verification, our monitoring teams are equipped to readily facilitate the new dynamics of clinical research sites with a focus on precise and meaningful data.

Triumpharma has also a network of Medical Doctors (MDs) that are available to provide 24/7/365 medical oversight of ongoing trials across a wide range of  .