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RIC REMS Stakeholder Survey 2023
Current
RIC - REMS Stakeholder Survey - 2023
Complete
This survey is intended to gather quantitative and qualitative feedback on REMS programs. It is intended to assist the RIC to understanding stakeholder perceptions of REMS programs in general and to identify topics for further research.
As a non-profit association that represents a wide array of organizations, our focus is on REMS programs generally and our questions are therefore focused on REMS programs
in the aggregate
, rather than any particular REMS program. Survey results may be shared with others, such as RIC member companies or FDA with pre-screening, so that any program-specific or company-specific references are removed.
Should you have feedback for specific REMS programs, we ask that you refrain from including that information in this survey response, and instead direct your comments to those who administer each individual REMS program.
By voluntarily submitting your responses, you are consenting to its use. You acknowledge and agree that we may preserve content and materials submitted by you. We may also disclose such content and materials if required by law or if, in our business judgment, such preservation or disclosure is reasonably necessary.
Contact Information
Name of Person or Organization Submitting Comments:
If Organization, Primary Contact Name
Email address:
Phone number:
Survey Questions
Would you or someone from your organization be willing to participate in additional discussions with RIC Work Groups?
Yes
No
Identify Stakeholder Type that best describes you
Identify Stakeholder Type that best describes you
- Select -
Patient
Pharmacy
Prescriber
Wholesaler-Distributor
Sponsor/Vendors
Other…
Enter other…
Identify Therapeutic Area(s) - SELECT ALL THAT APPLY
Allergy
Analgesia/Anesthesiology/Anti-inflammatory
Cardiology
Dermatology
Endocrinology/Metabolism/Bone
Gastroenterology
Hematology/Coagulation
Infectious Disease
Neurology
Oncology
Ophthalmology
Pain Management
Psychiatry
Pulmonary / Respiratory
Rheumatology
Other…
Enter other…
Which of the following aspects of REMS programs do you (or your organization’s members) directly engage with? (Select all that apply)
REMS Program enrollment (e.g. patients or healthcare providers)
Education / Training (e.g. that a REMS Program mandates for healthcare providers or patients)
Entering REMS Program-Required Information (e.g. lab tests)
REMS Authorizations
REMS Audits
Other…
Enter other…
How would you rate the effectiveness of REMS programs in identifying and addressing safety risks of prescription drugs and biologics?
How would you rate the ease of accessing information about REMS programs?
How satisfied are you with REMS programs that you have utilized from an overall perspective?
Independent of the benefit/risk profile of a product, has the existence of a REMS program ever impacted your decision about whether or not to prescribe or dispense a product? (e.g., changed to alternative product without REMS or from a Pharmacy perspective not to carry a product)
Yes
No
How often do you experience patient access issues (delays), due to REMS requirements?
- Select -
Always
Frequently
Sometimes
Never
What two areas do you see as being least burdensome/most effective for REMS programs generally?
REMS Program enrollment (e.g. patients or healthcare providers)
Education / Training (e.g. that a REMS Program mandates for healthcare providers or patients)
Entering REMS Program-Required Information (e.g. lab tests)
REMS Authorizations
REMS Audits
Other…
Enter other…
What two areas do you view as priorities for improvement?
REMS Program enrollment (e.g. patients or healthcare providers)
Education / Training (e.g. that a REMS Program mandates for healthcare providers or patients)
Entering REMS Program-Required Information (e.g. lab tests)
REMS Authorizations
REMS Audits
Other…
Enter other…
Submit
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