Welcome Your Participation as Guest Speaker for MEDTEC on-site Conference - KMPH FOX 26 | Central San Joaquin Valley News Source

Welcome Your Participation as Guest Speaker for MEDTEC on-site Conference

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SOURCE UBM China

-- MDiT Forum and Regulation Summit 2014

SHANGHAIJune 12, 2014 /PRNewswire/ -- Following the huge success of MEDTEC China on-site conference 2012 & 2013, MDiT Forum and Regulation Summit 2014 will continue to focus on regulatory updates & market access, product design & manufacture and risk management & quality control of medical devices. The conference will be held on September 25th-26th at Shanghai world Expo Exhibition & Convention Center which will continue with the theme of "Gearing up MD Development by Regulations & Innovations" which was very well-received by attendees in 2013, and will aim to provide to you the latest regulatory updates and advanced technology sharing. There are 4 Modules for this year:

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Module A: Chinese Regulatory Updates and Implementation

Module B: Design and Innovation of Medical Device Concept & Technology

Module C: Overseas Regulatory Updates and Market Access

Module D: Risk Management and Quality Control

Hot Topics

  • Updates of Regulations on Supervision and Administration of Medical Devices: New requirements for medical device manufacturers
  • Special Approval Process for Innovative Medical Device by CFDA, the main content and influence for manufacturers, how to take advantage of this policy?
  • Using a customer value-centric perspective to dissect customer expectations and transform them to exceed commercial expectations
  • Application of fast curing liquid medical silica gel in room temperature, high transparent silica gel and doped fiber high strength silica gel in medical device
  • FDA updates: Bringing clarity to the 510(K) modifications and IDE approval processes
  • UDI implementation and influence to manufacturers, how to avoid the common pitfalls
  • Risk analysis techniques and methodology for medical device and how to apply them to control product quality under ISO13485/QSR820
  • How to take measures to cooperate with unannounced inspection of FDA and what preparations should be made by manufacturers

Call for Speakers

UBM/MEDTEC is compiling a great roster of thought leaders and industry insiders for a program packed with timely insights, strategic views, and actionable items. If you would like the opportunity to speak at MEDTEC on-site conference 2014, please submit your proposed topic, biography and contact information to us.

Producer:

Ms. Jessie Jiang
jessie.jiang@ubm.com / +86 21 6157 3933

Sponsorship & Delegates:
Ms. Julia Zhu
Julia.zhu@ubm.com /+86 21 6157 3922

Ms. Heron Zhuang
Heron.zhuang@ubm.com /+86 21 6157 3928

Media & PR:

Ms. Alisha Zhou
Alisha.zhou@ubm.com /+86 21 6157 3930

(Logo: http://photos.prnasia.com/prnh/20140612/0861404094)

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