We are ready to perform for you a full range of bioequivalence “turn-key” studies, or each of the stages separately:
Development of study protocol / documents
Selection of the optimal design for your medicinal product, which allows you to avoid additional time and financial costs in the approve process
Organization of the experimental part of the study
Statistical processing of the results
Preparation of study reports
Our advantages
Extensive research experience
Performing clinical studies in a time efficient manner
Cost optimization
Please contact our team at . to discuss your specific needs and application.