Our experts develop the following documents:
Synopsis
Protocol
CRF
Information for the patient
Informed Consent
Final Report
In our Center, package of documents are developed by specialists with extensive experience in clinical trial documentation.
Our team engages in close collaboration with bioanalytical specialists, biostatisticians, physicians with expertise in various therapeutic areas of medicine, along with experts in analytics and statistics during the document development process.
Please contact our team at . to discuss your specific needs and applications.