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About QED Medical
QED Medical provides the medical device industry with regulatory, quality management and general product development advice. This includes device classification and regulatory strategy planning (Aus, EU, US), ISO 13485 internal auditing, technical file preparation, product development or manufacturing development documentation creation / review, implementing design controls to 21 CFR 820, clinical evaluation reports and risk management documentation, etc. The QED Mission is to measure, analyse and streamline projects and processes so that safe and effective, high quality medical products reach people who are in need of them as fast as possible.