Meet & Greet with Gert Bos at the CIMDR & One-to-One Consultation

August 17, 2017 / China

Qserve’s Executive Director & Partner, Gert Bos, has been invited to speak at the 8th China International Medical Device Regulatory Forum (CIMDR) that will take place on 15-18 August 2017 in Hangzhou, China.

Qserve’s agenda:

17 August 2017 

 

 18 August 2017 

Please note: One-To-One meeting sessions with Gert Bos available. 

Forum Language: English and Chinese Mainly, all venues are in English simultaneous interpretation.

Location: Hangzhou International Expo Center, China.

Online registration: By August 10, 2017

For more information and subscription, please visit the CIMDR website.

One-To-One Consultation Meeting

Introduction

Who could book the meeting:
Top Management 
Director of Regulatory Affairs
Quality Director
Director of Clinical Affairs
Director of Design & Development
Other management who’s involved in compliance of Medical device regulations

Language: English & Chinese
Date: 15-18 August 2017
Time of the session: 45 minutes per meeting
Location: Hangzhou International Expo. Center
Admission fee: 1,500 RMB

Topics could be covered including but not limited to following:
Key impacts of EU MDR/IVDR
Regulatory Strategy advice
Clinical evaluation / MEDDEV 2.7.1 Rev. 4 / Post Market Clinical Follow up
QMS / ISO 13485:2016 & MDSAP
UDI, traceability & transparent
PMS & Vigilance
Combined device
Notified Body Selection
Others related topics for medical device regulation compliance for key global markets

Please sign up here for the One-to-One Consultation Meeting.

Should you have any questions, please contact:

Booking Contact: Mrs. Minghua Chen
Mobile: 18061661543
Email: minghua.chen@qservegroup.com 


Profiles:

Gert W. Bos
Minghua Chen
Post date: July 25, 2017
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