FDAnews Announces -- China's NMPA (CFDA):Latest Regulatory Updates with QMS-PMS Focus Webinar January 21, 2020

Tuesday, January 7, 2020 Press Release
Email Print This Page Comment bookmark
Font : A-A+

Get clarity on the regulatory reform in China that impacts medical device and IVD industry. Sign up for our Jan. 21 webinar.

FALLS CHURCH, Va., Jan. 7, 2020 /PRNewswire-PRWeb/ -- China's NMPA (CFDA): Latest Regulatory Updates with QMS-PMS Focus An FDAnews Webinar Tuesday, Jan. 21, 2020, 11:00 a.m.-12:30 p.m. EST https://www.fdanews.com/chinanpma

China is the second-largest medical device and in vitro diagnostic (IVD) industry market globally. It is the only market with a 20 percent annual growth rate year after year.

Stay up to speed on the hundreds of new regulations introduced by China's National Medical Products Administration (NMPA) — formally known as the China Food and Drug Administration.

What are the strategic factors to consider during the reform before submission?

Join us on Jan. 21 and get up to speed on the regulatory reform in China that impacts the medical device and IVD industry.

During the webinar, attendees will:

  • Determine how to leverage a legal agent in China to increase compliance by understanding their roles and responsibilities
  • Discover how to assess and determine the new piloted MAH system by understanding its MAH qualification requirements and responsibilities
  • Familiarize oneself with how to leverage overseas QMS for China operations by understanding China GMP regulations and Chinese culture differences
  • Find out how to comply with required adverse events (AE) and serious adverse events (SAE) reports, including how to differentiate between AE and SAE and when to report
Join us for clarity on China's regulatory reforms impacting the medical device and IVD industry.

Interested in registering multiple sites? Call (888) 838-5578 in the U.S. or +1 (703) 538-7600 globally to learn about our special multisite discount.

Webinar Details: China's NMPA (CFDA): Latest Regulatory Updates with QMS-PMS Focus An FDAnews Webinar Tuesday, Jan. 21, 2020, 11:00 a.m.-12:30 p.m. EST https://www.fdanews.com/chinanpma

Tuition: $287 per site

Easy Ways to Register: Online: https://www.fdanews.com/chinanpma By phone: 888-838-5578 or 703-538-7600

About FDAnews: FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.

 

SOURCE FDAnews



Post your Comments

Comments should be on the topic and should not be abusive. The editorial team reserves the right to review and moderate the comments posted on the site.
* Your comment can be maximum of 2500 characters
I agree to the terms and conditions
Diabetes Premium Membership Benefits

News A - Z

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Search

Medindia Newsletters

Subscribe to our Free Newsletters!

Terms & Conditions and Privacy Policy.

Press Release Category

Press Release Archive

Stay Connected

  • Available on the Android Market
  • Available on the App Store