In accordance with medical device regulations, the confirmation of compliance with general safety and performance requirements, assessment of undesirable side effects and appropriateness of the risk-benefit ratio must be based on clinical data that provides sufficient clinical evidence. As a CRO specialized in clinical trials, ZURKO RESEARCH offers the following services:
We design, search for and select the most appropriate variables to assess the safety and efficacy of your product. Please contact us for a personalized study design.
Adverse effects
Tolerance
RSI scale
Patient acceptability