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AIMBE-FDA Workshop Survey

Regulatory Education in Engineering Programs

Thank you for providing your feedback on the recent workshop. 
1.Please rate the format of the workshop.
Strongly Agree
Agree
Neutral
Disagree
Strongly Disagree
There was a good balance between presentations and discussion.
The presentations were useful in sparking the discussions.
There was adequate representation from academia, FDA and industry for the presentations.
There was adequate representation from academia, FDA and industry in the small group discussions.
Adequate time was allowed for small group discussions.
Sufficient/appropriate guidance was provided for the small group discussions.
Adequate time was allowed for full group discussions
The format of presentations, followed by the small group discussions, wrapping up with the panel discussions was effective.
There was a reasonable amount of time allotted to each session.
2.Please rate the impact of the workshop.
Strongly Agree
Agree
Neutral
Disagree
Strongly Disagree
I will act on what was discussed/presented/learned.
I will suggest that my students become familiar with resources on the FDA Website for help in addressing regulatory aspects for projects/completing assignments.
I will suggest that my students contact the Division of Industry and Consumer Education (DICE) for help in addressing regulatory aspects for projects/completing assignments.
I will incorporate an expectation to use voluntary standards and FDA guidance documents to complete assignments/projects.
3.Please comment on next steps. 
Strongly Agree
Agree
Neutral
Disagree
Strongly Disagree
The next workshop should be on educating the educators.
The next workshop should focus on incorporating basic regulatory education in every program (i.e., “walking”).
The next workshop should focus on identifying and using available resources.
Future workshops should use a similar format.
Professional societies (e.g., BMES, SFB) should be involved in future workshops.
I would use an on-line repository of information (e.g., case studies, workshop presentations) to help incorporate regulatory education.
I have case studies or other tools (e.g., syllabus) I would contribute to an on-line repository of information to help incorporate regulatory education.
4.Please rate the facilities. 
Strongly Agree
Agree
Neutral
Disagree
Strongly Disagree
Although there are challenges associated with use of FDA facilities, significant attendance by FDA personnel is worth the effort.
The room set-up was conducive to discussion.
5.Please use this space to provide your feedback on the workshop format, impact, facilities, or other comments. 
6.Please complete your contact information if you wish to share with other participants.
7.I would like to volunteer to help with writing a white paper on the workshop discussions. (If yes is selected, make sure your contact information is recorded in the previous question.)
Current Progress,
0 of 7 answered