E-Learning Of Regulatory Affairs Of Medical Device

E-Learning Of Regulatory Affairs Of Medical Device - Printable Version

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E-Learning Of Regulatory Affairs Of Medical Device - Courses24h - 12-25-2024

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[h1]Free Download E-Learning Of Regulatory Affairs Of Medical Device[/h1]
Published: 12/2024
MP4 | Video: h264, 1920x1080 | Audio: AAC, 44.1 KHz
Language: English | Size: 205.81 MB | Duration: 0h 36m
Embrace regulatory joy of medical device

[h2]What you'll learn[/h2]
Learn how to register medical device in international markets
Optimise the compilation of technical documentation
Manange of regulatory affairs skills
Know regulatory intelligence of medical device
[h2]Requirements[/h2]
basic knowledge of medical device
eager to have intercultural communication
[h2]Description[/h2]
We want to share regulatory intelligence with you indepedent in which career level you are staying at medtech. You will learn registration pathway from EU, MDR to US, FDA and CN NMPA etc...Learning audienceStudent and unemployed:Basic knowledge for Chinese registrationNon Medtech personal:Gain [h3]Overview[/h3] and tactic of Chinese market entry, useful for publication (medical writers)Non Regulatory personal Tongue

erfect for career changerRegulatory professionals:Either with or without experience of registration, improve registration efficiency, ideal as boot camp for RA groupOn website of easychinapprov, you can select any session what you wish to learnSession: Chinese accessSession: Registration in ChinaSession: Chinese Post market and quality managementSession: Global marketsSession: Regulatory Affairs Soft SkillsSession: FDA and CanadaSession: CE cerfiticationSession: Singapore, Malaysia and VietnamSession: TaiwanEach session is made of script, video, test and case study. In professional modul you can have face to face coach with our best chosen regulatory expert.Start: Participation possible any time.Duration: 1 yearHow to start: Kick off meeting with trainer, book trainingEnd of E-Learning: for professional user there is test, free supervision hours and certificateProof of E-learningA certificate will be issued after successful test for each session and qualitative homework.
[h3]Overview[/h3]
Section 1: [h3]Overview[/h3] of international registration of medical device
Lecture 1 From MDR to Chinese market of medical device
Lecture 2 From FDA to Chinese market of medical device
Section 2: Workflow of Chinese registration
Lecture 3 Pathway of Chinese registration
Lecture 4 Type testing
Section 3: Our Service
Lecture 5 E-Learning of regulatory affairs
Student,Junior regulatory affairs manager,Career changer in medtech

Homepage:

Code:
https://www.udemy.com/course/e-learning-of-regulatory-affairs-of-medical-device/

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