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Clinical Trial Documents Development

PHARMBIOTEST has experience in clinical trials and provides document development services for phase I-IV clinical trials, including bioequivalence studies.


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 to discuss your specific needs and application.

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