Our Solutions | Med Clinical Research

Clinical Data Management

We bridge the gap from start-up to close-out and make the clinical trial experience efficient and compliant. In our efforts to remain environmentally friendly, our preferred sites uses e-source to provide on time, real-time data for every project.

Co-monitoring Services

We are ready and willing to get the job done whether you need just a little or a lot of help. Our team of dedicated clinical research professionals will get you back on track, giving you the support to meet your project goals.

Ongoing Study Management

If you need to outsource a portion of your study, or require full service provider services, we are just a phone call away. Our team of dedicated study Managers will work in synergy with your project team to ensure site management activities like site qualification, site initiation, routine monitoring and close-out visits meet project timelines.

Study feasibility and start up

We help our clients find the missing piece to the puzzle. Our team of clinical monitors will work to protect your investment by providing a realistic assessment and capability to conduct the clinical trial.

Training and Site Audit

Our clinic sites are registered members of the Society of Clinical Research Sites and all trainings are ACRP approved. Training is the backbone of any properly executed clinical study and we take training very seriously. If you need to get your associate up to speed in no time, look no further, we are just a phone call away.

We exist and operate in a regulated industry and therefore all clinical trials must be in compliance with ICH-GCP, FDA code of federal regulations as well as local regulations. All site audit are conducted by certified quality assurance experts.