STUDY MONITORING

Our clinical monitoring service is conducted by an exceptionally experienced team – all our CRAs have worked in Clinical Research for at least 7 years.

Because our Senior Managers have worked as researchers within the NHS, they are able to build strong and effective working relationships with hospital study personnel based on mutual respect. This ensures that we achieve optimal results from our carefully selected investigative sites. We are ideally placed to rapidly identify potential issues and deal with them accordingly.

Our team has worked on a wide variety of clinical studies. This means we are accustomed to modifying our approach to monitoring and query resolution to encompass differing levels of Source Data Verification and risk-based monitoring strategies.

In addition to the dataMagik solution, we have worked with a broad range of EDC and paper-based systems.

With our wealth of knowledge in managing study protocols and experience of compliance with MHRA, FDA & EMEA requirements, TCRS ensures that your study rigorously adheres to all relevant directives.

The TCRS study monitoring service also includes drug accountability and, if required, we can implement strategies to increase patient recruitment and retention. Strategic analysis will be performed throughout the project life cycle to ensure it is on track.