Medelis provides specialized oncology consulting services for both large and small sponsors needing that outside perspective to resolve current challenges in the clinic, or to develop the right protocol to maximize outcomes.
We specialize in oncology, and our entire team has deep oncology trial experience and expertise — from our world-class medical advisory board to our clinical team members and medical personnel. This critical first-hand experience in the complex issues often associated with oncology clinical trials
Our team has handled most targets within oncology. Whether it’s navigating the FDA regulatory maze, optimizing a standard dose-escalation phase I trial or a complex rescue of a phase III trial, chances are that our team has handled it before.
In addition to our oncology consulting services, we provide a single-source oncology contract research organization for clinical trial planning, trial management and drug development planning for sponsors running clinical studies in North America and Europe.
Our services:
Our clinical team’s comprehension of the complex issues of oncology trials translates into better problem identification, decision making and superior results. We value innovation, and our experience allows us to work smarter, to maximize cost and time efficiencies on your trial.
We’re flexible, collaborative and proactive, and able to quickly adapt to study challenges or changes in the regulatory or competitive environment. This helps to speed a drug to market, and provides the decision support to determine your next clinical move.
Contact us to learn more about how we’re helping sponsors bring oncology drugs to market.
Tell us more about your drug development needs or current study challenges.