Free Webinar: China Medical Device Regulatory YearReport-2015

CIRS is glad to offer the China medical device regulatory yearly report of 2015 and make it into a free webinar. This webinar will focus on the overview of regulations of medical devices during 2015, including the new implemented regulations, the submission and registration summary, adverse events, the review of big events and so on.

If you are a manufacturer or distributor involved in exporting medical device or IVDs to China, this webinar will provide you with very valuable information to tell you what was happening in China of 2015 and what is going to happen in China of 2016. Professional suggestions/opinion will also be given for your reference according to our enormous practical experiences.

Topics Covered

An overview of CFDA new implemented regulations, standards and guidelines in 2015
Summarize the CFDA registration number of medical device in 2015 (category: domestic, imported, Class I, Class II, Class III, withdrawal)
Review the adverse events, recalls and violations
Latest update of CFDA approved testing center and laboratories
How clinical trial evaluation guideline works under the new regulations
Close reading of some big events
What is going to attract your attention in 2016

Time and Schedule

Time: 25^thFeb 2016, Thursday.Two webinars will be offered in consideration of different time zone.
Webinar 1 (English): Asian (GMT+8) 3:00-4:00 pm;
Webinar 2 (English): Europe (GMT) 4:00-5:00 pm; America (PST) 8:00-9:00; America (CST) 11:00-12:00.
Presentation Focus: a systemic regulatory yearly report of medical devices of 2015, tell those you would be interested in
Presenter: Mr. Michael Petersen
Registration fee: Free of charge;

About the Presenter

Michael Petersen | 上官福调
Senior Consultant of Medical Device Legislation Compliance
Mr. Michael Petersen is a Senior Consultant in the Medical Device Legislation Compliance Department of CIRS, he gained his master degree (Biomedical Engineer) from University of Columbia-Missouri in 2010. Michael has an extensive background in China medical device regulatory activities by developing compliance procedures for medical device registration in CFDA, compliance procedures for the entry of medical device and formulated technical methods for the regulatory risk management in China. He is as well as focused on the tracking and update of CFDA medical device regulations, deliver newsletter and significant info to clients.

Who Shall Attend

Manufacturers and distributors who export medical device or IVDs to China;
CEO who has plan to sell your medical devices into China;
Regulatory affairs specialist - healthcare;
Quality assurance/control professionals

How to Register

After online registration, you will receive a link one day and one hour before the webinar starts. By clicking that link, you shall be able to join our webinar automatically

Webinar Link：

Webinar 1 (English): 3:00-4:00 pm (GMT+8);
Registration URL:
https://attendee.gotowebinar.com/register/2629520912793236482
Webinar ID: 102-439-299

Webinar 2 (English): 4:00-5:00 pm (GMT) ;
Registration URL:
https://attendee.gotowebinar.com/register/4574919821166432002
Webinar ID: 106-461-147

Note: To attend this seminar, there is no need to call dial-in telephone number to access audio
Please note that space is limited.

Contact Us
Ms. Windy Jin,Windy@cirs-group.com
11F Building 1, Dongguan Hi-Tech Park, 288Qiuyi Road, Binjiang District, Hangzhou 310052, China
Tel: +86-571 8720 6559 | Fax: +86-571 8720 6533

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