functions
as defined in Commission Implementing Regulation (EU) No 920/2013 of 24 September 2013 on the…, Article 1, point (j) (Definitions)
the tasks to be fulfilled by the body’s staff and its external experts, namely: auditing of the quality systems, product related technical documentation review, review of clinical evaluations and investigations, device testing and, for each of the previously mentioned items, the final review and decision making thereon