Clinical Operations & Study Start-Up
Cmed knows clinical trials. We understand that clinical studies for your product make up the most expensive, labor-intensive and time-consuming component of your development process. And the clinical development landscape just keeps getting more complex:
> Expanding geographical spread of sites.
> More complicated clinical study protocols.
> Increased regulatory agency expectations.
> Stringent post-marketing commitments.
> Continuing adoption and adaption of industry standards and best practices.
One sure constant is that time is of the essence. Getting your trial complete on time is critical to realizing your investment – and more importantly, to helping patients that need your treatments.
How we ensure excellence in delivery
> We focus on excellence in delivery while maintaining the integrity of your
> Our transparent approach combines tried and true methods of program
management, study start-up and clinical monitoring.
> We build strong partnerships based on open, honest communication and
on teamwork to deliver successful outcomes.
> We work in tandem with each study site to ensure that patient safety and
standard of care practices are the first priority.
Our people are our success
Cmed’s highly experienced clinical project managers lead teams built based on the needs of your project – so you’ll have the right skills at the right time. And the staff assigned to your trial is dedicated to you throughout the life of your study! This is how Cmed is able to design and deliver on your program in this increasingly challenging space.
For more information contact:
Vice President, Clinical and Regulatory Operations
+1 919 595 6900