Risk Evaluation and Mitigation Strategy (REMS) Programs to Promote Appropriate Medication Use and Knowledge: Patient Experiences with REMS Programs
Dear [Patient Support Group Name] Members,
I am a faculty member at Harvard Medical School and Brigham and Women’s Hospital, and I am conducting research on Risk Evaluation and Mitigation Strategy (REMS) programs, which the Food and Drug Administration (FDA) requires the manufacturers of certain medications to implement. My project team and I are seeking to better understand the benefits and burdens of REMS programs on patient care. Our work is being funded by the FDA and does not involve any pharmaceutical companies.
We would like to extend an invitation to those of you who are 18 years or over who have started taking or care for someone who has started taking [drug name]—a REMS program-covered drug—in the past year to participate in a 60-minute phone interview on your experiences. Your participation is voluntary. If you choose not to take part, it will not affect your affiliation with your support group in any way. If you choose to take part, your answers will be treated confidentially, and you will receive a $50 Amazon gift card as a token of appreciation for your participation.
If you meet the above condition and are interested in participating in the study, please email me at [email protected] with the subject line “REMS Patient Interview.”
Thank you very much for your consideration of this invitation.
Best,
Ameet Sarpatwari, Ph.D., J.D.
Assistant Professor of Medicine at Harvard Medical School
Division of Pharmacoepidemiology and Pharmacoeconomics
Brigham and Women's Hospital
1620 Tremont St, Suite 3030
Boston MA 02120
File Type | application/vnd.openxmlformats-officedocument.wordprocessingml.document |
Author | Mayookha Mitra-Majumdar |
File Modified | 0000-00-00 |
File Created | 2022-06-06 |