Recorded Webinars

Recorded Webinars

China IVD Registration Pitfalls and COVID-19 Test Kit Updates

08/17/2020

Practical Lessons for Coronavirus Related Products Fast Track Clearance in China

Mandatory Period Risk Evaluation & latest PMS Requirements

07/09/2020

China Mandatory Period Risk Evaluation Report and the latest PMS Requirements in NMPA and FDA

Update on China NMPA & US FDA Emergency Approval

04/08/2020

Update on China NMPA & US FDA Emergency Approval - Implications to Life Science Companies Relating to COVID-19

2019 NMPA (CFDA) Key Updates & Trends: Look Ahead to 2020

01/27/2020

2019 NMPA (CFDA) Key Updates & Trends: Look Ahead to 2020

China’s NMPA Latest Regulatory Updates with PMS QMS Focus

01/23/2020

China’s NMPA Latest Regulatory Updates with PMS QMS Focus

Developments in Clinical Pathways for NMPA (CFDA) Submission

12/02/2019

Clinical Pathways for NMPA Image

China Adverse Event and Post Market Surveillance

06/17/2019

Illustration of a laptop computer showing Grace Fu Palma speaking during a presentation for a webinar

How to Navigate Type Testing in China

04/04/2019

Era of Transformation 2018 NMPA (CFDA) Major Regulation Updates

12/27/2018

NMPA (CFDA) Overseas Inspection Video

08/16/2018

Key Ingredients for Effective NMPA (CFDA) CER & Clinical Trial

06/13/2018

CFDA-clinical-requirements-for-medical-device-and-IVD-have-been-evolving

Success Factors In China MedTech Market

05/03/2018

Webinar-Success-Factors-in-China-Medtech-Market

How To Get IVD Approval Through NMPA (CFDA)

01/17/2018

NMPA (CFDA) Key Updates GMP/QMS Overview

01/31/2017

Illustration of a laptop computer showing Grace Fu Palma speaking during a presentation for a webinar