Studies to Enhance FDA Communications Addressing Biosimilar Drug Products: Focus Groups and INterviews with Healthcare Professionals

Data to Support Drug Product Communications

Consent Form individual interviews

Studies to Enhance FDA Communications Addressing Biosimilar Drug Products: Focus Groups and INterviews with Healthcare Professionals

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Informed Consent Form: HCP Individual Interviews


Introduction and Purpose:

Thank you for agreeing to participate in this research study. The purpose of the study is to obtain healthcare professionals’ feedback on educational materials about a type of biologic drug product called biosimilars. Fors Marsh Group (FMG), a research organization in Arlington, VA, is conducting this study sponsored by the US Food and Drug Administration (FDA).


Procedures:

You will take part in a one-on-one interview during which we will show some written materials on your computer screen and ask you questions about them. The interview will be conducted online using a video and audio platform so you will be able to see and talk with the moderator. The interview will last about 90 minutes.


Benefits:

There is no direct benefit to you for participating. However, what we learn from the interviews will help the FDA more effectively communicate with healthcare professionals, patients and the public about biologics.


Risks/Discomforts:

There are no known risks to participating in this study. You do not have to answer any questions that you don’t want to answer. You can also stop participating in the interview at any time. Your participation is completely voluntary.


Confidentiality:

Your identity and information will remain private to the extent permitted by law. Your personal information (name, address, phone number) will not be linked to any of your responses. The information you provide will be combined with the responses of other participants in a summary report that will not identify you by name.


We will audio- and video-record the discussion to supplement our notes and to ensure your comments are accurately captured. Recordings and transcripts will not include full names or any other personally identifiable information, and they will be stored on password protected computers at FDA and FMG that only project staff can access. FMG will retain these files for three years and then delete them. You will not be contacted in the future about this study after your participation in this interview ends.


Honorarium:

In appreciation for your time and participation, you will receive an honorarium of $250 following the interview. In line with the usual process, you will see this honorarium reflected in your account on the All Global Circle portal within one week after completing the interview.



Right to Refuse or Withdraw:

Your participation in this study is voluntary. You can choose not to talk about any topic, and you can withdraw from the interview for any reason at any time without penalty or loss of the honorarium.


Observation:

Some research team members from FMG and FDA will observe the interview through video streaming. They will not record your name and will keep all of your comments confidential.


Persons to Contact:

If you have questions or concerns about the interview, you can contact Dr. Brian Griepentrog at FMG by email at [email protected] or by phone at 571-858-3757. If you have questions about your rights as a study participant, concerns about how you are treated in the study, or want to report an injury from the study, contact the FDA’s Research Involving Human Subjects Committee (RIHSC) at [email protected] or 301-796-9605.


We advise you to keep a copy of this consent form for future reference. If you would like to do so, print a copy now.


Your Consent:

I have read this consent form. I agree to be audio- and video-recorded. I had a chance to ask questions, and my questions were answered. I was given the opportunity to print or save a copy of this consent form. I agree to participate in the study.


By clicking “yes” below, you are consenting to participate. If you click on “no” below, you are not consenting to participate in an interview.

I have read and understand the information provided above, and the study’s purpose and procedures are clear to me.

Shape1 Yes, I agree to participate in this study.
Shape2 No, I do not wish to participate in this study.

 

Signature:

Shape3

Date:

Shape4



File Typeapplication/vnd.openxmlformats-officedocument.wordprocessingml.document
File TitleChildren’s Book Testing focus group consent form
Authorbkelly
File Modified0000-00-00
File Created2021-01-21

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