POST-MARKETING DRUG SAFETY RESEARCH: ANALYSIS OF RECOMMENDATIONS OF FOREIGN REGULATORS

• Main Authors: E. V. Shubnikova (Author), T. M. Bukatina (Author), D. A. Kaperko (Author), N. Yu. Velts (Author), M. A. Darmostukova (Author), A. S. Kazakov (Author), I. I. Snegireva (Author), E. O. Zhuravleva (Author), G. V. Kutekhova (Author)
• Format: Book
• Published: Ministry of Health of the Russian Federation, Federal State Budgetary Institution «Scientific Centre for Expert Evaluation of Medicinal Products», 2018-09-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

The monitoring of information on the safety of various drugs is becoming more relevant day by day, as the number of drugs on the  pharmaceutical market increases, generic drugs, bio-analogous drugs appear. Long-term post-marketing use of a  medicinal product allows to accumulate a sufficient evidenc...