In today’s demanding clinical trial environment, there is no alternative for knowledge and experience. Therapeutic area expertise is particularly important as pharmaceutical and nutraceutical companies develop new classes of compounds that target complex and difficult diseases.
At Pepgra we specialize in providing sound therapeutic expertise to support your clinical studies, and we offer comprehensive therapeutic expertise across a wide variety of indications. Pepgra shapes its clinical trials services to meet your needs. We can provide complete program development, delivery services for any part of a trial that you are looking to outsource or even save failing trials. With our experienced clinical research, medical and scientific professionals, we have an in-depth knowledge that allows us to apply new concepts and innovation into clinical trials.
Our teams include experienced clinical research associates, project managers, medical supervisors, data management experts, biostatisticians and medical writers. These experts are available at every stage of the clinical development process: early-phase studies, pivotal trial planning and design, protocol development, safety narratives, In-house data summaries, safety surveillance plan, case Report Form, site selection, data analysis, and regulatory submissions.
Our therapeutic area expertise is essential to designing cost-effective clinical research trials that deliver the data you need to support your novel therapies.