Methodological Approaches to Evaluate the Impact of Risk Evaluation and Mitigation Strategy (REMS) Programs: Physician Interviews on Experiences with REMS Programs
Dear [Dr. X],
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 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 conducted on behalf of the FDA and does not involve any pharmaceutical companies.
We are requesting your help as someone who might have prescribed [drug name]—a REMS program-covered drug—in the last year. If so, we would like to invite you to participate in a 60-minute phone interview about your experiences. Should you choose to take part, your answers will be treated confidentially, and you will receive a $100 Amazon gift card as a token of appreciation for your participation. Our work is being conducted on behalf of the FDA and does not involve any pharmaceutical companies. You can find more details in the accompanying Consent Form.
If you meet the above condition and are interested in participating in the study, please email me at asarpatwari@bwh.harvard.edu with the subject line “REMS Patient Interview.”
Thank you very much for your consideration of our 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 | 2022-05-23 |