We offer research support services to researchers delivered by a team of competent academic scholars with a special interest in research methodology and extensive national and international experience.
Every clinical investigation begins with the development of a clinical protocol. The protocol is a document that describes how a clinical trial will be conducted (the objective(s), design, methodology, statistical considerations and organization of a clinical trial,) and ensures the safety of the trial subjects and integrity of the data collected. Our Medical Writers become an extension of your team by being flexible to your scope, using our expertise to guide you through your clinical data and demonstrate the efficacy of your drug and improve patient safety. We have a wide breadth of knowledge and experience drawn from the pharmaceutical industry, clinical research organizations, and academia. All documents produced by SevoClin undergo thorough scientific, statistical, editorial and quality control review.
I like to work with this wonderful team for their commitment to schedule and deadlines.
The work was above and beyond what I could have expected. Great job!.
Excellent service all the way around from start to finish. Keep up the Great work!
SEVO-Clin is a contract research organization company. We have the expertise in regulatory requirements, and clinical trial management and have an unparalleled track record of success.
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