ASSOCIATION OF MEDICAL DIAGNOSTICS MANUFACTURERS
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2022 AMDM Hybrid Focus Meeting Evaluation
Thank you for taking the time to submit your 2022 Hybrid Focus Meeting Evaluation. Please use the following rating system when assigning a value to each presenter.
1=Unsatisfactory
2=Fair
3=Satisfactory
4=Good
5=Excellent
Day 1
Legislative Update - John Stone
*
5
4
3
2
1
General Update - Vivian Ngan-Winward
*
5
4
3
2
1
IVDR in Clinical Trials - Camilla Recke
*
5
4
3
2
1
NGS Panels - Eunice Lee
*
5
4
3
2
1
CLIA LDT vs IVD Reporting - Jennifer Dickey
*
5
4
3
2
1
QSR and ISO 13485 - Josh Levin
*
5
4
3
2
1
Guidance: Conducting Remote Assessments - Jamie Wolszon
*
5
4
3
2
1
Regulatory Options for Novel Markers - Erika Ammirati
*
5
4
3
2
1
Navigating Clinical & Regulatory Efforts - Carol Chen
*
5
4
3
2
1
Breakthrough Device Designation - Michelle Roeding
*
5
4
3
2
1
Day 2
FDA’s Oncology Center... - Lynne McBride
*
5
4
3
2
1
Developing Assays.. - Megan Doyle
*
5
4
3
2
1
Industry Update - Allyson Mullen
*
5
4
3
2
1
Review of First NGS Group Claim - Anika Schaedle
*
5
4
3
2
1
US Reimbursement - Tom Hughes
*
5
4
3
2
1
Please rate the overall event on format & organization
*
5
4
3
2
1
Please rate the overall event on overall relevance / value
*
5
4
3
2
1
Please tell us your years of regulatory experience
*
Less than 1 year
1-5 years
6-12 years
13-19 years
20+ years
What suggestions for improvements or additions to the program would you offer?
*
What speakers/topics would you like to suggest for future programs?
*
Submit
About
Board
Scholarships
Contact
Members
Join
Jobs
Networking
April Meetings
Meetings
Meetings
Webinar Registration
Roundtables
Past Presentations
RA/QA Topics
Resources
Store