FDAnews Announces — Medical Device Package and Labeling Compliance Under EU-MDR …

Action plans to update artwork and labels for IVDD devices by May 2022 and class IIa and IIb devices by May 2023; How other medical device …

The EU-MDR labeling and packaging standards require major changes. This webinar has the details needed to comply. Register today.

FALLS CHURCH, Va. (PRWEB) November 06, 2020

Medical Device Package and Labeling Compliance Under EU-MDR

An FDAnews Webinar

Wednesday, Nov. 20, 2020, 11:00 a.m.-12:30 p.m. EST

https://www.fdanews.com/mdpackagelabeling

Ready for the EU-MDR changes to labels and packaging? Is one’s quality management system fully integrated to move toward compliance?

This Medical Device Package and Labeling Compliance Under EU-MDR webinar on Nov. 20 will help provide the answers one needs. With expert insights, attendees will gain a better understanding of artwork and labeling compliance and determine how to best move forward.

Bob Tilling, Business Development Manager at Kallik, and Simon Hoffman, Principal Quality Assurance and Regulatory Affairs Consultant, will share tips on meeting the key labeling requirements for the new EU-MDR. They’ll talk about ways companies have managed the transition and implemented systemic solutions for moving forward.

During this webinar, they’ll cover:

  • Key labeling and overall requirements for the EU-MDR
  • Action plans to update artwork and labels for IVDD devices by May 2022 and class IIa and IIb devices by May 2023
  • How other medical device companies have risen to the challenge of compliance by using technology to proof artwork and label regulation changes
  • The transition between the MDD and the MDR
  • Full, systemic solutions that integrate with a quality management system and company operations
  • Ongoing regulatory, industry and customer requirements
  • The best way to achieve full compliance without detriment to customer and patient delivery, avoiding the traditional reactive compliance approach

Get the knowledge needed to ensure packing compliance by registering for this webinar.

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:

Medical Device Package and Labeling Compliance Under EU-MDR

An FDAnews Webinar

Wednesday, Nov. 20, 2020, 11:00 a.m.-12:30 p.m. EST

https://www.fdanews.com/mdpackagelabeling

Tuition:

$287 per site

Easy Ways to Register:

Online: https://www.fdanews.com/mdpackagelabeling

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

For the original version on PRWeb visit: https://www.prweb.com/releases/fdanews_announces_medical_device_package_and_labeling_compliance_under_eu_mdr_webinar_nov_20_2020/prweb17529771.htm