Attach importance to sources: understand and evaluate the sources of clinical data. Give priority to the materials published by authoritative medical journals, academic conferences or reliable medical institutions.
Verify data: For research results or clinical data, you can try to verify its accuracy. This can be achieved by consulting the repeatability of relevant research and checking the rationality of sample number and method.
Consider study design: Evaluate the design of clinical study, including sample size, random grouping, control group, etc. More reliable research design is helpful to improve the reliability of data.
Statistical analysis: understand the statistical methods and analysis process used in the study. Reasonable statistical methods can improve the reliability of research and reduce possible deviations.
Expert review: solicit expert opinions and reviews, especially materials involving complex clinical problems or controversial conclusions. Expert review can provide valuable advice on reliability and interpretation data.
Independent research: look for other independent research or viewpoints to understand the consistency and coherence between different viewpoints. Multiple independent studies with similar conclusions can improve the reliability of data. Pay attention to quality standards: for clinical guidelines, expert knowledge and systematic review, pay attention to the quality standards and evaluation process on which they are based. Authoritative guidelines and knowledge are often strictly evaluated and reviewed.
It should be pointed out that evaluating the reliability of clinical data is a complex process, which requires comprehensive consideration of multiple factors. At the same time, it is also important to understand clinical research methods and scientific principles, as well as to have critical thinking and information discrimination ability. Before making a decision or taking action, it is best to have further consultation and discussion with medical professionals or reliable information sources.
For medical devices that submit clinical trial data of similar products, the clinical trial data shall include: clinical trial reports or related clinical documents of similar products that have been listed by this enterprise or other enterprises, and compare them with similar products (including basic principles, main technical performance indicators, expected uses, etc.). ).