• Effective clinical
    planning, execution
    and management

  • Clinical Monitoring

Clinical Monitoring

Clinical Research Associates (CRAs) are the foundation for successful delivery of your trial. Cmed’s seasoned CRAs are dedicated to the integrity of your study data and patient safety, ensuring quality through both onsite and remote monitoring. Site investigators and teams consistently tells us that they value the partnerships our CRAs establish and the demonstrated level of skill and commitment brought to their sites.


Our CRAs:

>  Have the experience and skills to deliver trials within a wide
    range of therapeutic areas, including indications that are rare
    and highly complex to treat.

>  Understand the standards of care associated with each trial and
    importance of patient safety; site management is a holistic
    approach to ensuring regulatory and study compliance is maintained.

>  Have a turnover rate well below industry average, a testament to
    both the culture at Cmed and the great working relationship they have
    with our sites and customers.