{"id":559788,"date":"2024-03-20T22:15:00","date_gmt":"2024-03-21T02:15:00","guid":{"rendered":"https:\/\/platohealth.ai\/2024-national-inspection-plan-released-today-pay-attention-to-your-device-standards\/"},"modified":"2024-03-21T01:14:53","modified_gmt":"2024-03-21T05:14:53","slug":"2024-national-inspection-plan-released-today-pay-attention-to-your-device-standards","status":"publish","type":"post","link":"https:\/\/platohealth.ai\/2024-national-inspection-plan-released-today-pay-attention-to-your-device-standards\/","title":{"rendered":"2024 National Inspection Plan Released Today: Pay Attention to Your Device Standards","gt_translate_keys":[{"key":"rendered","format":"text"}]},"content":{"rendered":"
NMPA announced the \u201c2024 National Inspection Plan for Medical Devices\u201d today on March 19, 2024. The Plan asks provincial NMPA offices and testing centers to conduct quality inspections based on Mandatory Standards and Product Technical Requirements (PTRs).<\/a><\/p>\n The plan covers 66 medical devices and IVDs<\/a>, including but are not limited to the following. NMPA lists the inspection items, referenced by mandatory standards, for each product. Email info@ChinaMedDevice.com<\/a> if you have any devices as following in China market.<\/p>\n The Plan also lists institutions and procedures for inspection, retesting and appealing.<\/p>\n Whether you are renewing or submitting new registration, your medical devices need to meet new mandatory standards. Even if your renewals (every 5 years required by NMPA) have no changes, you still have to prove that your originally approved products can meet the new standards. As a result, your originally approved products will still need to go through local type testing to show that you are current with the new standards.<\/p>\n China Med Device, LLC has test engineers on-site at NMPA testing centers to help you assess and expedite your type testing needs and shorten your renewal or new approval time.<\/p>\n NMPA announced the \u201c2024 National Inspection Plan for Medical Devices\u201d today on March 19, 2024. The Plan asks provincial NMPA offices and testing centers to conduct quality inspections based on Mandatory Standards and Product Technical Requirements (PTRs). Full List The plan covers 66 medical devices and IVDs, including but are not limited to the following. […]<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":2,"featured_media":559791,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[52],"tags":[],"acf":[],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"https:\/\/platohealth.ai\/wp-json\/wp\/v2\/posts\/559788"}],"collection":[{"href":"https:\/\/platohealth.ai\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/platohealth.ai\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/platohealth.ai\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/platohealth.ai\/wp-json\/wp\/v2\/comments?post=559788"}],"version-history":[{"count":1,"href":"https:\/\/platohealth.ai\/wp-json\/wp\/v2\/posts\/559788\/revisions"}],"predecessor-version":[{"id":559790,"href":"https:\/\/platohealth.ai\/wp-json\/wp\/v2\/posts\/559788\/revisions\/559790"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/platohealth.ai\/wp-json\/wp\/v2\/media\/559791"}],"wp:attachment":[{"href":"https:\/\/platohealth.ai\/wp-json\/wp\/v2\/media?parent=559788"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/platohealth.ai\/wp-json\/wp\/v2\/categories?post=559788"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/platohealth.ai\/wp-json\/wp\/v2\/tags?post=559788"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}Full List<\/h3>\n
\n
Mandatory Standards<\/h3>\n
\n