CDBMCO
Biomedical Research Consulting
Clinical Trial Management • Monitoring • Medical Writing
CDBMCo offers Clinical Development expertise to serve delivery of your clinical studies.
Whether you are a Biotech, a Pharmaceutical corporation or an Academic organization we can help you move your projects forward.
Get in touch with us today to discuss your projects and your needs.
Building effective teams, structured project and alignment are our 3 pillars to conduct projects. We lead your teams through operational set-up of the trials, provide structured planning and budgeting, manage outsourced activities, in respect with ethical and regulatory requirements.
At CDBMCo we conduct the clinical trials combining our love for project management, with our 20-year experience in multiple indications and therapeutic areas, translational medicine and pediatric development.
We’re proud to help shape and improve how our clients structure and manage their business.
A robust study design and a well-written protocol are first key components of successful trials. With our 20-years experience in several therapeutic areas and interacting with regulatory authorities, we aim to deliver protocol packages in line with quality standards, ethical and regulatory requirements.
We also provide the following services (and more): data medical review, Scientific Committees or Data Safety Monitoring Boards management, Key Opinion Leaders interviews, Patient Reported Outcomes set-up.
Delivering robust study data is our goal. With our extensive knowledge in Clinical Trial conduct, we understand that Quality is not only a requirement from Health Authorities, it lessens stress within teams, foster enthusiasm and save time. We work with your Management board and your cross-functionnal teams to create your standards operating procedures, structure the methods, and implement preventive.
