A webinar was held on the topic “Analysis of medical research”, fully compliant with ISO 13485 and ISO 14971 standards

Med Quality conducted a training session on “Risk Analysis of Medical Devices in Compliance with ISO 13485 and ISO 14971 Requirements.” The webinar was led by the company’s director, Vladislav Kasyanenko, who has many years of experience in medical device conformity assessment. The training covered key ISO standards, including ISO 14971, and discussed approaches to risk management throughout the medical device lifecycle. Special attention was given to methods for reducing residual risk and the risk-benefit analysis process. This training was an important step in raising participants’ awareness of medical device safety issues.