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Develop study-related protocols, case report forms (CRFs) and database tools for records management.

Determine the safety and effectiveness of medications and medical devices.

Communicate scientific, technical and health-related information to a range of audiences.

Make clear and accurate presentations of scientific and technical data.

Creation of clinical protocol document which details how a clinical trial is designed, relating to to the methodology, hypothesis, and operation of clinical trial to ensure the safety of the patients is maintained as well as maintaining the integrity of the data collected during the trial.

Database or collection of data related to health outcomes directly reported by the patient who experienced it, without interpretation of the patient's response by a clinician or anyone else.

Database containing, through utilizing observational research methods, standardized data about patients who have the same condition, disease, or exposure and is used to evaluate an outcome

Trial Insights is the industry’s first digital research reporting dashboard made specifically to track ongoing clinical trials, observational, diagnostic and medical device studies. The solution aggregates and curates content from multiple public data sources to provide comprehensive, customizable dashboard reports, updated in real-time. <br> <br> <iframe width="560" height="315" src="https://www.youtube.com/embed/NjVS4Ri9Ogo" frameborder="0" allow="accelerometer; autoplay; encrypted-media; gyroscope; picture-in-picture" allowfullscreen></iframe>

Training for medical science liaisons who want to work in pharmaceutical, biotechnology, medical device, and managed care companies.

Support services for Medical Science Liaisons (MSL).