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[Webinar] Revisiting 2022 And Looking Into 2023: Regulatory Updates For Medical Device Market Access In China

Register Here Schedule: CountryUS & CanadaEuropeChinaScheduleWednesday February 15 8:00am-9:00am PDT, 11:00am – 12:00pm EDTWednesday February 15 5:00pm-6:00pm CETThursday February 16 12:00am-1:00am China time Description: Medical device manufacturers who are dedicated to bringing their products to the Chinese market may need…

[Webinar] Keep Up With The Trend Of Medical Devices Localization In China: Background, Policy, Regulation, And Case Study

Register Here Topic: Keep up with the Trend of Medical Devices Localization in China:Background, Policy, Regulation, and Case Study Schedule: CountryUS & CanadaEuropeChinaScheduleWed, November 27:00am-8:00am PDT,10:00am – 11:00am EDTWed, November 24:00pm-5:00pm CETWed, November 210:00pm-11:00pm Beijing Time Description: Since the release…

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

Register Here: Time Option 1 Time Option 2 Topic: Medical Device Real World Evidence (RWE) in China: Policies, Usage, Study Plan, Case Study Schedule: CountryUS & CanadaEuropeChinaTime Option 1Wed, Jun 157:00am-8:00am PDT,10:00am – 11:00am EDTWed, Jun 154:00pm-5:00pm CETWed, Jun 1510:00pm-11:00pm…

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

Wednesday, April 27, 2022, 8:00-9:00 AM Pacific Time (US and Canada)

Register Here Topic: China Regulatory Updates of Q1/2022 & Tips for Medical Device Registration under Covid Date: Wednesday, April 27, 2022, 8:00-9:00 AM Pacific Time (US and Canada) As we entered year 3 of the Covid pandemic, China medical device…

[Webinar] How To Increase The Likelihood Of China CER Approval?

Wednesday, Feb 23, 2022, 8:00-9:00 AM Pacific Time (US and Canada)

Register Now Topic: How to increase the likelihood of China CER approval? Date: Wednesday, Feb 23, 2022, 8:00-9:00 AM Pacific Time (US and Canada) Clinical evaluation is mandatory for getting market approval in China for Class II or III medical…

[Webinar] Keep Up With The Enhancement Of Medical Device Post-Market Surveillance In China: GMP, GSP, And NMPA Onsite Inspections

Tuesday, January 11, 2022, 8:00-9:00 AM Pacific Time (US and Canada)

Register Now Date Tuesday, January 11, 2022, 8:00-9:00 AM Pacific Time (US and Canada) Summary Since the implementation of Order 739 Regulations on Supervision and Administration of Medical Devices in June 2021, China continues to enhance post-market surveillance on medical…

[Webinar] Revisiting Order 739 – Significant Updates For Medical Device Registration In China: Dossier Prep, Self-Testing, CER, And PMS

Thursday, Nov 18, 2021, 8:00-9:00 AM Pacific Time (US)

Register Now Date: Thursday, Nov 18, 2021, 8:00-9:00 AM Pacific Time (US) 2021 is a big year for medical devices in China. Issued by the State Council, Order 739 (“Regulations on the Supervision and Administration of Medical Devices”) was officially…

[Webinar] Expediting The Registration Of Respiratory Equipment And Patient Monitoring Devices In China: Insights, Challenges, And Solutions

Friday, August 20, 2021, 7:00-8:00 AM Pacific Time (US and Canada)

Register Now Topic: Expediting the Registration of Respiratory Equipment and Patient Monitoring Devices in China: Insights, Challenges, and Solutions Date: Friday, August 20, 2021, 7:00-8:00 AM Pacific Time (US and Canada) In the context of COVID-19, the demand for respiratory…

[Webinar] China Modified MDR (Order 739) Has Arrived— Opportunity Knocks: Quality Management System, Design Control, Post-Market Surveillance

Thursday, September 2, 2021, 7:00-8:00 AM Pacific Time (US and Canada)

Register Now Date: Thursday, September 2, 2021, 7:00-8:00 AM Pacific Time (US and Canada) Summary: With the implementation of Order 739 in July 2021, China National Medical Product Administration (NMPA) continues to strengthen the product lifecycle supervision and impose heavier…