Patient Device Label Survey

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* 1. About the Process Making Device Label Rules - How important is it to:

  Unimportant Matters a little Important More than average Very Important
Include patients in the process of creating label regulations.
Have standard formats for elements of device labels, like tables of contents.
Adjust label requirements for risk, less rules for low risk devices.
Keep process simple enough to avoid fueling cost increases to comply with rules.

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* 2. About What is in Device Labels: How important are:

  Unimportant Matters a little Important More than average Very Important
Clear instructions for use and risk.
Have standard formats for elements of device labels, like tables of contents.
Frequently Asked Questions.
Have clear uniform instructions for reporting device errors to FDA.
Outlining the information needed for a meaningful device event report.

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* 3. About Accessing Device Labels: How important are:

  Unimportant Matters a little Important More than average Very Important
There is a printed copy that comes with the devices.
Access to a customer support phone number
Make a copy available online
Provide online support center 
Image based instructions
Multilingual resources

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* 4. Do you have any other comments, questions, or concerns?

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* 5. Please let me know you contact information and I'll share the survey results.

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