« Previous
Next »
Titles
- 30-Day notices, 135-day premarket approval (PMA) supplements and 75-day humanitarian device exemption (HDE) supplements for manufacturing method or process changes: guidance for industry and Food and Drug Administration staff1
- A few states fell short in timely investigation of the most serious nursing home complaints: 2011-20151
- A short case record in psychiatry, with a moral: a morbidly sensitive moral sense1
- Expiration dating of unit-dose repackaged solid oral dosage form drug products1
- FDA drug approval: application review times largely reflect FDA goals : report to Congressional requesters1
- FDA drug approval: application review times largely reflect agency goals : report to Congressional requesters1
- Mammography technique1
- The principles of the chrono-thermal system of medicine: with the fallacies of the faculty, in a series of lectures1
- Traumatic and chemical asphyxiation, part 21
- VA construction: actions taken to improve Denver Medical Center and other large projects' cost estimates and schedules : testimony before the Committee on Veterans' Affairs, U.S. House of Representatives1
- VA health care: opportunities exist for improving implementation and oversight of enrollment processes for veterans : report to Congressional committees1
- Veterans crisis line: further efforts needed to improve service : statement for the record for the Committee on Veterans' Affairs, House of Representatives1
- Veterans health care: VA actions needed to ensure timely scheduling of specialty care appointments : report to congressional committees1
- Veterans' health care: preliminary observations on veterans' access to choice program care : testimony before the Committee on Veterans' Affairs, House of Representatives1