The proper design of a clinical investigation plan is essential for medical device manufacturers, since poorly designed plans can result in data that fail to sufficiently support a manufacturer’s safety and/or performance claims. In some cases, an iso 14155:2011 clinical investigation plan fails to identify rules and procedures for the collection of data. In other instances, the sample size identified in the plan is not based on scientific and statistical principles but solely on a manufacturer’s experience. In other cases, the investigation plan fails to select a study protocol that minimizes sample bias. These and other flaws in the design of a clinical investigation of medical devices plan can impede the regulatory approval process and delay market access.
At a minimum, a clinical investigation of medical devices must follow a proper risk management process to identify all possible risks associated with a medical device, and be appropriately designed to collect clinical data relevant to the safety and performance of the device. ISO 14155:2011, Clinical Investigation of Medical Devices for Human Subjects – Good Clinical Practice, provides detailed information regarding clinical investigation principles, the process of conducting a clinical investigation, and the information to be collected. A clinical investigation plan designed to comply with the requirements of this standard helps to ensure the collection of objective and credible scientific data and supports the overall goal of protecting the safety and well-being of patients.
TÜV SÜD Product Service experts can conduct a voluntary pre-assessment of a manufacturer’s medical device clinical investigation plan in advance of execution. In addition, TÜV SÜD Product Service has a global staff of medical device specialists, with over 400 international experts located in major markets around the world. These specialists are supported by the in-house clinical affairs department and the scientific advisory board that is under the standard TÜV SÜD confidentiality agreement. This board comprise well-recognized European scientists and physicians from the leading universities and healthcare centers.
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