Audit of the registration dossier

Before submitting the registration dossier to the regulatory body it is recommended to assess the completeness, completeness, and correctness of the documents included in the registration dossier for compliance with the national/EAEU requirements, depending on the country chosen and the registration procedure in force at the moment.

RECOMMENDATIONS FOR THE CONDUCT OF CLINICAL/NONCLINICAL TRIALS

EVALUATION OF THE DOCUMENTS INCLUDED IN THE DOSSIER

RECOMMENDATIONS FOR THE STATE REGISTRATION PROCEDURE

Employees of X7 Research can conduct a qualitative analysis of the dossier for compliance with all regulatory requirements. After the review, the client receives recommendations for each section of the registration dossier, which further helps to minimize the risks of submitting the registration dossier to the regulatory body

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