Name *

First Name

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Content Relevance to Industry Insights *

Please rate the extent to which our publication effectively addresses regulatory, reimbursement, and policy issues in the medtech industry.

5 — Highly Relevant

4 — Somewhat Relevant

3 — Neutral

2 — Somewhat Irrelevant

1 — Irrelevant

Depth of Analysis and Information *

How would you rate the depth and comprehensiveness of the analysis provided in our publication regarding regulatory, reimbursement, and policy issues in the medtech sector?

5 — Very Comprehensive

4 — Somewhat Comprehensive

3 — Neutral

2 — Somewhat Insufficient

1 — Very Insufficient

Usability and Actionability of Insights *

Rate the usability of the insights provided in our publication – whether it offers practical guidance for navigating regulatory challenges and policy changes in medtech.

5 — Very Helpful

4 — Somewhat Helpful

3 — Neutral

2 — Somewhat Unhelpful

1 — Very Unhelpful

Content Access/Format Preferences *

Please rate your preference for accessing our publication in both print and digital formats.

5 — Strongly Prefer Digital

4 — Somewhat Prefer Digital

3 — Prefer both Print & Digital

2 — Somewhat Prefer Print

1 — Strongly Prefer Print

Content Readability and Navigation *

How would you rate the readability and ease of navigation in both the print and digital versions of our publication?

5 — Easy to Read/Navigate

4 — Somewhat Easy to Read/Navigate

3 — Neutral

2 — Somewhat Difficult to Read/Navigate

1 — Difficult to Read/Navigate

Overall Satisfaction *

Considering both print and digital formats, please rate your overall satisfaction with our publication.

5 — Very Satisfied

4 — Somewhat Satisfied

3 — Neutral

2 — Somewhat Unsatisfied

1 — Not Satisfied

What recurring features in Market Pathways do you find most valuable? *

Select at least 1

Consultants Corner

Document Depot

FDA Output

Global Spotlight

Market Pathways Scorecard

Medtech Law & Policy

Pathways Picks

Please select any topics you are most interested in *

Select at least 1

Regulation

Reimbursement

Quality/Compliance

Diagnostics

Digital Health

Clinical Trials

Legislation

Health Technology Assessments

FDA

CMS

Europe MDR and IVDR

Asia

Other (Please describe in Gen. Feedback)