QST Consultations has provided specialized clinical research support for the pharmaceutical and medical device industries since its founding in 1974 (incorporation in 1985). QST specializes in clinical study design, protocol development including statistical methodology, clinical operations, data management, biostatistical analysis, report writing, and FDA consultation.
We strive to find the perfect solution for all of our sponsors, from small startup organizations to established pharmaceutical leaders. We know that each trial is unique, and our staff brings its decades of technical expertise to tailor our solutions to meet the specific needs of each client.
In additional to a wide range of quality control, programming, medical writing and other support services, our work blends on-going marketing activities and many successful Phase I-III and Post-Marketing clinical trials crafted to support a number of FDA pharmaceutical and medical device submission requirements, including:
- 510(k) Premarket Notifications
- Premarket Approval Applications (PMA)
- Abbreviated New Drug Application (ANDA)
- New Drug Application (NDA)
Michigan 50 - 2013 Awardee
QST Consultations, Ltd. was selected as one of Michigan's 50 Companies to Watch and was honored at an awards ceremony during the ninth annual Michigan Celebrates Small Business event, May 2, 2013 in Lansing, Mich.
Read more »