Table 3.
Statement | Important/Extremely Important | Selected as Being in the Three Most Important Statements |
---|---|---|
Tracking safety events with biosimilars | 99% | 49% |
Access to information on studies comparing biosimilars with reference biologics | 96% | 54% |
Establish reasonable and scientifically justified approach to interchangeability and automatic substitution | 93% | 53% |
Physician authority to decide on the most suitable biologic for each patient | 89% | 47% |
Knowledge about biosimilars among interdisciplinary colleagues | 86% | 24% |
Preparing (educating about biosimilars, which includes patients) to integrate biosimilars into clinical practice | 84% | 18% |
Switching between reference biologics and biosimilars | 74% | 19% |
Naming conventions for biosimilars (unique vs. same non-proprietary names) | 74% | 16% |
Tender policy with preference for Russian manufacturers | 54% | 19% |
Data were extracted from question 11 of the questionnaire (see Survey Questionnaire 1).