Biostatistics for Medical Device Clinical Trials
Our Ph.D. and Master's-level biostatisticians play a critical role in the application of statistical and research methodological principles for the design, execution and analysis of medical device clinical trials. They work closely with clients to ensure that clinical studies are conducted in accordance with regulatory requirements and client objectives.
MDCI provides a variety of biostatistics support for all phases of pre-clinical studies and clinical trials, including:
- Pre-clinical and clinical program consultation
- Protocol design, development and statistical analysis plan development to ensure consistency with the final protocol
- Randomization schemes and sample size justification
- Generation of statistical summary tables, graphs and reports using SAS for regulatory submissions, presentations, and publications
- Interim and final statistical analysis and reporting
Contact MDCI today to learn more about our Biostatistics for Medical Device Clinical Trials.
Contact Us
Reach our Massachusetts office at 1-508-643-0434, Monday through Friday, 9:00 a.m. to 5:00 p.m. Eastern. Or fill out our contact form and a consultant will contact you directly.
Client Testimonial
The expertise and knowledge that MDCI shared truly helps us accomplish our mission of helping U.S. companies increase their export sales.
- International Trade Specialist at US Department of Commerce