Medical Viewpoints provides experienced independent contract research consultants for clinical research and medical monitoring in the conduct of clinical trials for new pharmaceuticals and medical devices. A clinical research associate and a medical monitor with a combined experience of 26 years are available to provide careful and detailed onsite monitoring anywhere in the United States to include pre-study site evaluation, study initiation, data review and retrieval, as well as quality and regulatory assurance. In addition, medical monitoring is available to retrieve completely and accurately all serious adverse events, and to interact with study investigators and CRA's to resolve any clinical questions that may arise during each trial. We are experienced in working closely with study sponsors and Contract Research Organizations and communicating on a real time basis.

Medical Viewpoints provides experience in all phases of clinical trials ranging form initial planning to assistance in the preparation of the final study report for submission. We also are available for trouble shooting difficult sites and reviewing and retrieving data from sites that have had previous substandard record keeping.

Our clinical experience extends into almost all therapeutic areas and pharmaceutical applications. We are proud of our participation in many clinical trials that have led to the successful approval of products in a variety of therapeutic areas. Please review our resumes and if you need more information, please use the contact page of this site to reach us.