Consulting services

QBIO ensures full compliance of the clinical development parameters of the investigational product with the regulatory requirements of the Eurasian Union.
SERVICES

Consulting

The decision to conduct clinical trials in a new region or country is not only a solution to the problems of regulatory support and obtaining research approval. When conducting a clinical trial, the organization faces many issues: from importing the study drug and exporting biological samples to the specifics of interacting with medical organizations, research centers and patient organizations. We provide comprehensive advice on all these issues.

GET HELP FROM OUR CONSULTANTS

Plan clinical trials in our region
Select research centers and local suppliers
Coordinate and finalize agreements with counterparts
Obtain permission to import study drugs
Obtain permits to export biological samples
CONSULT AN EXPERT

CONTACTS US

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