Medical device registration company, medical device third party registration service, medical device business license processing center, Hangzhou certification standard guest Enterprise Management Co., Ltd. official website

Registration Service of Medical Devices: CRC services Medical Device Business License Medical Device Registration Contract Research Organization ISO 13485 Quality System Certification GMP CE Certification Service FDA Registration (Filing) Software Integrity Verification Service Production process validation service ISO 15378 Medical Package System Certification ISO 13485 Internal Auditors Training Regulatory Services For Medical Devices
Information security service of medical: ISO 27001 Information Security Certification ISO 20000 Information Service Certification Information system grade protection filing Business Continuity Management Services Internal Auditor Training
Medical Software Development: Software of Good Supply Practice(GSP) Production System Development Customized software development

Current location: Default>Services>FDA Registration (Filing)

FDA 510(k) 注册流程 FDA是食品药品监督管理局（Food and Drug Administration）的简称。FDA有时也代表美国FDA，是国际医疗审核权威机构，由美国国会即联邦政府授权，专门从事食品与药品管理的最高执法机关。对于生产II类医疗器械的生产商来说，需要在美国食品药品管理局(FDA) 申请市场准入，即FDA 510K申请。只有通过美国FDA注册认证，才能获得在美国合法的销售许可。 Time:2018-6-29 11:34:46 View:2444