Clinical Monitoring
Clinical Monitoring
Pharmedas physicians and other clinical operation personnel are always in hand to provide support in the planning, conduct, and evaluation of clinical trials. We will provide the insight that will help in designing a robust study by critically appraising all sections of the protocol. Our project team members can combine to deliver high quality medical Monitoring, training and support, protocol reviews, investigator engagement, data reviews, safety analyses and study reports. Our medical staff are knowledgeable and well-trained and have the expertise to support Phase II-IV clinical studies up to the point of regulatory submission.
Our approach to monitoring of clinical studies is proactive, risk-based and adaptive. At Pharmedas, we put patients first. Our monitors and medical leads are always on the lookout for pointers of issues that may impact on the study. These are analysed with the sponsor so that appropriate actions are taken.