000			02969cam a2200361 i 4500
999			_c2086 _d2086
001			4380113
005			20200922150712.0
008			911010m19929999nyua b 001 0 eng c
020			_a0824785762 (v. 1 : alk. paper)
020			_a0824787714 (v. 2 : alk. paper)
020			_a0824790200 (v. 3 : alk. paper)
040			_aDNLM/DLC _cDLC _dDLC _erda
082	0	0	_a615.19 _220 _bP
245	0	0	_aPharmaceutical dosage forms : _bparenteral medications / _cedited by Kenneth E. Avis, Herbert A. Lieberman, Leon Lachman.
250			_aSecond edition., revised and expanded.
264		1	_aNew York : _bM. Dekker, _c[1992-1993].
300			_a3 volume . : _billustrations ; _c26 cm
336			_2rdacontent _atext
337			_2rdamedia _aunmediated
338			_2rdacarrier _avolume
504			_aIncludes bibliographical references and index.
505	2		_aVolume 1: -- 1. The parenteral dosage form and its historical development -- 2. Parenteral drug administration: Routes, precautions, problems, complications, and drug delivery systems -- 3. Biopharmaceutics of injectable medications -- 4. Preformulation research of parenteral medications -- 5. Formulation of small volume parenterals -- 6. Formulation of large volume parenterals -- 7. Parenteral products of peptides and proteins -- 8. Sterile diagnostics -- 9. Glass containers for parenterals -- 10. Use of plastics for parenteral packaging -- 11. Elastomeric closures for parenterals -- 12. Parenteral products in hospital and home care -- Volume 2: -- 1. The processing of small volume parenterals and related sterile products -- 2. Factors involved in manufacturing large volume parenterals -- 3. Freeze drying: Principles and practice -- 4. Design considerations for a parenteral production facility -- 5. Biopharmaceutical manufacturing facility design -- 6. Personnel: The key factor in clean room operations -- 7. Environmental control in parenteral drug manufacturing -- 8. Industrial sterilization: A review of current principles and practices -- 9. Development of ophthalmic formulations -- Volume 3: -- 1. Quality assurance -- 2. Records and reports -- 3. Particulate matter -- 4. Validation of sterilization processes and sterile products -- 5. Federal regulation of parenterals -- 6. Systematic audits of parenteral drug good manufacturing practices -- 7. Medical devices: Design, manufacture, and quality control -- 8. Quality assurance for medical devices -- 9. Regulatory and GMP considerations for medical devices.
650		0	_aParenteral solutions.
650		0	_aPharmaceutical technology.
650		2	_aInfusions, Parenteral.
650		2	_aTechnology, Pharmaceutical.
700	1		_aAvis, Kenneth E., _d1918-, _928032 _eeditor.
700	1		_aLieberman, Herbert A., _d1920-, _928033 _eeditor.
700	1		_aLachman, Leon, _d1929-, _928034
856	4	2	_3Publisher description _uhttp://www.loc.gov/catdir/enhancements/fy0647/91038063-d.html
942			_cBK _2ddc