000			00318nam a2200121Ia 4500
999			_c146684 _d146684
040			_cCUS
082			_a615.191 _bLIE/P
100			_aLieberman, H. A
245		0	_aPharmaceutical dosage forms/ _cH. A Lieberman
250			_a2nd ed.
260			_aNew York: _bMarcel Dekker, _c2005.
505			_aChapter 1 Quality Assurance / Samir A. Hanna -- chapter 2 Records and Reports / David C. Fry Karl L. Hofmann -- chapter 3 Particulate Matter / Patrick P. DeLuca Julius Z. Knapp -- chapter 4 Validation of Sterilization Processes and Sterile Products / James Agalloco James Akers -- chapter 5 Federal Regulation of Parenterals / Terry E. Munson Jonas L. Bassen Bernard T. Loftus -- chapter 6 Systematic Audits of Parenteral Drug Good Manufacturing Practices / Ronald F. Tetzlaff -- chapter 7 Medical Devices: Design, Manufacture, and Quality Control / David H. Wayt -- chapter 8 Quality Assurance for Medical Devices / Carl W. Bruch -- chapter 9 Regulatory and GMP Considerations for Medical Devices / Larry R. Pilot.
650			_a Parenteral solutions
650			_aPharmaceutical technology.
942			_cWB16