Our experts develop the following documents:
Synopsis
Protocol
CRF
Information for the patient
Informed Consent
Final Report
In our Center, the development of a package of documents is carried out by specialists with experience in developing a package of documents for clinical trials.
When developing documents, they work closely with bioanalyst specialists, biostatistics, physicians who have scientific knowledge in various therapeutic areas of medicine, analytics, and statistics.
Please contact our team at contact@pharmbiotest.com.ua to discuss your specific needs and application.