« Previous
Next »
Titles
- Part D plans generally include drugs commonly used by dual eligibles: 20171
- Pediatric information for x-ray imaging device premarket notifications: guidance for industry and Food and Drug Administration staff1
- Pediatric trauma centers: availability, outcomes, and federal support related to pediatric trauma care : report to Congressional requesters1
- Personal firearms: programs that promote safe storage and research on their effectiveness : report to Congressional requesters1
- Physician workforce: locations and types of graduate training were largely unchanged, and federal efforts may not be sufficient to meet needs : report to Congressional requesters1
- Potential misclassifications reported by drug manufacturers may have led to $1 billion in lost Medicaid rebates1
- Procedures for meetings of the Medical Devices Advisory Committee: guidance for industry and Food and Drug Administration staff1
- Product labeling for certain ultrasonic surgical aspirator devices: guidance for Industry and Food and Drug Administration staff1
- Product name placement, size, and prominence in promotional labeling and advertisements1
- Providing regulatory submissions in electronic format--certain human pharmaceutical product applications and related submissions using the eCTD specifications1
- Public health information technology: HHS has made little progress toward implementing enhanced situational awareness network capabilities : report to Congressional committees1