QTS

A Cretex Medical company

  • Our Approach
  • Services
    • Pre-Validated Medical Packaging
    • Package Design Expertise
    • Materials Sourcing
    • Engineering Validations
    • Label Development & Printing
    • Critical Inspection Services
    • Cleaning & Passivation
    • Cleanroom Assembly, Kitting & Packaging
    • Sterilization Services
    • Lab Testing Services
    • Supply Chain Management
  • Quality
    • Procedural Guidelines
  • Resources
  • News & Events
  • About
    • Vision and Values
    • Leadership
    • Power of Cretex Medical
  • Contact
  • Careers
  • News
  • Events
  • Blog

MDR Workshop

January 25, 2019 by QTS Medical Device Outsourcing

February 19, 2019 — Winona Lake, IN

QTS will be joining forces with Nelson Labs and DuPont to bring you a complimentary one-day seminar to learn more about the new European Medical Device Regulation (EU MDR). Our educational sessions will help better prepare you for upcoming changes and requirements in the marketplace and how they directly impact your medical device packaging, labeling, and validations.

Date/Time:

Tuessday, February 19
11:30 AM – 4:30 PM

Location:

Grace College (Westminster Hall)
105 9th Street
Winona Lake, IN 46590

Agenda:
11:30am – Registration & Lunch
12:00pm – Welcome
12:10pm – The New EU MDR/IVDR: The Impact on Sterile Packaging and Global Sterile Packaging Standards (DuPont)
1:10pm – Are Your Labels MDR Ready? (QTS)
2:10pm – MDR Effects on Cleaning and Sterilization Validations (Nelson Labs)
3:10pm – ISO 10993 & MDR Requirements: What You Need to Know (Nelson Labs)
4:00pm – Q&A Session and Event Wrap-Up

Note: Lunch and beverages are included.

Space is limited, so be sure to reserve your seat now!

Registration Button

Filed Under: Events

test

Stay informed on industry news.

Register here

Upcoming Events

  • MD&M West 2023
  • the[PACK]out 2023
  • OMTEC 2023
View Events »

Blog

  • Changing European Regulatory Requirements: Will your Medical Product be Affected?
  • What is Operational Excellence, and why is it Important to QTS?
  • QTS Collaborates with Other Industry Experts to Publish Best Practices Article on Tests of Sterility for EO Sterilization
View Blog »

Latest News

  • QTS Celebrates 20 Years in Business
  • QTS receives Global First in Sterile Device Packaging from MedAccred
  • QTS Presidential Transition
View News »

More Info

For more information on our services:

Contact us Download brochure

  • Terms of Use Policy
  • Website Privacy Policy
ISO 13485 Certified ISO 13485 Certified Med Accred Sterile Device Packaging

FDA Registered | J-PMDA Compliant


© 2023 Quality Tech Services, LLC