• Service
  • Resources
    • Webinars
    • Upcoming Events
    • Documents Download
    • FAQ
    • NMPA Approval Report
  • News
  • CER
  • About
Subscribe

Our Services

Strategy Consulting

  • Market Entry Strategy
  • Regulatory Strategy
  • Clinical Strategy
  • China Localization Strategy
  • Hainan Urgent Use Pathway
  • Innovation Pathway
  • Fast Track Pathway
  • Digital Health Consulting

Registration Affairs

  • Pre-market Registration
  • Modification Registration
  • Renewal Registration
  • Request for Classification
  • Legal Agent Representation
  • NMPA Expert Panel Meeting
  • NMPA Supplemental Notice

Quality Assurance

  • Postmarket Surveillance Compliance (IFU, Label, GSP)
  • Adverse Event Reporting
  • Recall Handling
  • Periodic Risk Evaluation Report
  • Annual QMS Self-Inspection Report
  • NMPA Inspections & Mock-Audit
  • QMS Establishment/Audit/Remediation
  • QA Gap Analysis
  • Factory Audit
  • Unique Device Identifier

Device Testing

  • China Local Type Testing
  • Device Modification Compliance Testing
  • Biocompatibility Testing
  • EMC Testing

Clinical Research Organization (CRO)

  • Clinical Trials/Research
  • Real-World Study
  • China CER & MDR CER
  • Clinical Evaluation Feasibility Assessment

Customized Training

  • China Regulatory Training
  • China QMS Training
  • China GCP Training
  • China Localization Training
  • Periodic Regulatory Updates Training

Other Services

  • Translation
  • Patent & Trademark
  • Distributor Evaluation & Audit
  • KOL Interview/Consultation
  • Investment
  • Global regulatory services
  • Service
  • Resources
    • Resources
    • Webinars
    • Upcoming Events
    • Documents Download
    • FAQ
    • NMPA Approval Report
  • News
  • About
  • CER
  • Subscribe
  • CN
  • US
  • Home
  • Short Videos
  • Webinars

Webinars


  • Webinars
  • Revisiting Order 739
  • Order 739
  • Clinical Evaluation
  • QMS&PMS
  • Respiratory Registration
  • China GMP/GSP/NMPA Onsite Inspections
  • Short Videos
  • China Localization

Introduction Of Medical Device Registration Process In China

2022-10-12

This shortvideo is the introduction of medical device registration process in China. First, we need be clear that…

READ MORE >

Medical Device Real World Evidence (RWE) In China: Policies, Usage, Study Plan, Case Study

2022-06-23

Part 1: Overview of policies, regulations, and guidelines of RWE in China Firstly, the speaker uses a graph…

READ MORE >

China Regulatory Updates Of Q1/2022 & Tips For Medical Device Registration Under Covid

2022-05-07

Part 1: 2022 National Medical Device Quality Sampling Inspection The speaker talks around 2022 national medical device quality…

READ MORE >

Unique Device Identification In China

2022-03-23

This short video discusses Unique Device Identification in China. It begins by explaining what UDI of medical devices means.…

READ MORE >

Part 5 Major Differences Between A China CER And An EU CER

2022-03-01

The speaker use a table to show major differences between a China CER and an EU CER.

READ MORE >

Part 4 Good Practice As Well As Pitfalls In Preparing A China CER

2022-03-01

There is a common review inquires for CER via Equivalence, for example, it list the following ppoints: study…

READ MORE >

Part 3 How To Prepare A Convincing China CER

2022-03-01

The speaker draw a outline CER outline to clarify how to prepare a convincing China CER. Then, it…

READ MORE >

Part 2 Have You Chosen The Best Clinical Pathway To Register Your Products In China?

2022-03-01

The speaker use a diagram to illustrate the clinical pathway under order 680. Then, it talks about least…

READ MORE >

Part 1 Major Changes To Clinical Evaluation Under Order 739

2022-03-01

The speaker talks about the changes under order 739 which is clinical evaluation for the whole life cycle.…

READ MORE >

Part 5 Case Study

2022-01-21

This section used some cases to explain. Such as overseas production site inspection of Boston Scientific Corporation, Becton…

READ MORE >

Part 4 GSP Inspection Observations And Corrective Measures

2022-01-21

More and more international companies set up the legal agent in China, so this section is helpful to…

READ MORE >

Part 3 Various Types Of NMPA Inspections On The Quality System Of Imported/domestic Medical Device Manufactures

2022-01-21

Firstly, it talks about inspection type of the quality system of overseas medical device manufactures by China NMPA,…

READ MORE >

Prev12345Next
Twitter Linkedin
United States
Email: info@bradyknowsmedical.com
Phone: +86 18600392020
China
Beijing Office: Room 1501-1502, East Ocean Centre, No. 24 A, Jianguomenwai Avenue, Chaoyang District, Beijing, China
Shanghai Office: Lingang New Zone, China (Shanghai) Pilot Free Trade Zone
Hainan Office: Boao Lecheng pilot zone of international medical tourism, Qionghai City, Hainan Province
Email: info@bradyknowsmedical.com
Phone: +86 18600392020 +86 10 65155991

©2025 Bradynuoen Beijing PharmTech Co Ltd All Rights Reserved.

京ICP备15042665号-7