The Importance of Effective Medical Device Reporting
If your company continues to struggle with the decision-making process of identifying when an adverse event should be reported, has trouble making MDR decisions due to difficulty in interpreting key terminology, or if your company is looking for industry and FDA guidance on the MDR process, this CD is definitely for you!
SPEAKERS
- Annette Hillring, President, Hillring & Associates, Inc.
- Deborah Yoder, Nurse Consultant, US Food and Drug Administration, Center for Devices and Radiological Health, Reporting Systems Monitoring Branch
- Victoria Schmid, Consumer Safety Officer, US Food and Drug Administration, Center for Devices and Radiological Health, Reporting Systems Monitoring Branch
PROGRAM-AT-A-GLANCE
- Overview of MDR regulatory requirements - the basics of 21 CFR 803
- Review of definitions of key terminology
- Discussion on the difficulties manufacturers encounter in the decision-making process and tips on how to avoid them
- Suggestions on effective MDR activities
- Review of current guidance documents available to provide industry assistance
WEBINAR CD
- Includes handout material and CD
- $245 for webinar registrants/ $345 for non-registrants
- Please note that domestic and international shipping rates apply
THREE WAYS TO ORDER
- Phone - 1-877-249-8226 / 240-646-7031 to order with credit card
- Fax - Select and download the order form and fax to 240-396-5781
- Mail - Select and download the order form and mail with payment to:
MDR Webinar CD Package
AAMI Publications
PO Box 0211
Annapolis Junction, MD 20701-0211
QUESTIONS?
For questions about ordering the CD, please contact AAMI Publications at 1-877-249-8226 / 240-646-7031.