NMPA Reviewer Q&A–Common Questions Faced In China Registration 2021-09-14 What should be considered in the heat treatment process of additive manufacturing—selective laser melting metallic materials for removable… READ MORE > Q&A For Expediting The Registration Of Respiratory Equipment And Patient Monitoring Devices In China 2021-09-14 1.What's the registration unit rule under Chinese regulation for ventilators? A ventilator is a pulmonary ventilation device used… READ MORE > NMPA Reviewer Q&A 2021/9/10 2021-09-10 To evaluate the virus inactivation effect, whether the animal-based medical devices must be subject to laboratory validation of… READ MORE > NMPA Reviewer Q&A 2021/9/7 2021-09-07 If a registered product does not apply for renewal registration within the specified time, can the original registered… READ MORE > NMPA Reviewer Q&A 2021/9/6 2021-09-07 1.If the registrant claims that a new clinical function of a medical device with software is a minor… READ MORE > NMPA Reviewer Q&A 2021/08/12 2021-08-12 Under what circumstances can a third-party institution / laboratory be entrusted with the testing of comparative methods in… READ MORE > FAQ-Clinical Evaluation Report 2021-08-12 Question: which of the requirements are obligatory regulation only? or all the standards?Answer: Order 739 is the regulation,… READ MORE >