Food and Drug Administration (FDA)
- Cover Letter to HDMA Comments to FDA on the REMS for Certain Opioids - June 30, 2009
- HDMA Comments on the FDA REMS for Certain Opioids - June 30, 2009
- HDMA Comments to FDA and OMB on MedGuide Paperwork Requirements - December 23, 2008
- HDMA Comments on REMS Under FDAAA - September 22, 2008
- HDMA Public Comments on the draft FDA Five-Year Plan for PDUFA Implementation - June 20, 2008
- HDMA Testimony at Joint FDA Advisory Committee Meeting on iPLEDGE - August 1, 2007
- HDMA Written Comments on Risk Minimization Action Plans (RiskMAPs) - July 27, 2007
- Distributors' Perspective on the Implementation of Risk Minimization Action Plans (RiskMAPs) - June 25, 2007
- HDMA Written Comments on Electronic Prescribing Information - June 22, 2007
- HDMA Testifies at FDA's MedGuide Hearing 6-13-07 - June 18, 2007
- HDMA Testifies on Electronic Prescribing Information Distribution - April 27, 2007
- Agenda for the FDA Public Hearing on Electronic Prescribing Information - April 27, 2007
- HDMA Comments on the Proposed NDC Rule - January 26, 2007
- HDMA Testimony on FDA's Proposed NDC Rule - December 11, 2006
- Patient
Safety Implications on Implementation of the Current FDA-Mandated
Medication Guide Program -
June 27, 2006
Consumer Product Safety Commission (CPSC)
Centers for Medicare and Medicaid Services (CMS)
Department of Defense (DoD)
Environmental Protection Agency (EPA)
The Office of Mangement and Budget
Contacts
Anita Ducca
Senior Director, Regulatory Affairs
703-885-0240
aducca@hdmanet.org
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