The following document provides UNFPA’s technical requirements in the procurement of medical devices (medical equipment, renewable medical supplies, and medical kits excluding pharmaceuticals that might accompany kits). It is intended to give to submitters all the necessary information for them to complete understandable and homogenous dossiers. From a general standpoint, UNFPA’s technical requirements are based on the current standards and regulations, for both the manufacturer’s quality assurance and devices compliance.
