000 01108nam a2200217Ia 4500
003 NULRC
005 20250520094922.0
008 250520s9999 xx 000 0 und d
020 _a824785940
040 _cNULRC
050 _aRS 189 .W55 1992
100 _aWillig, Sidney H.
_eauthor
245 0 _aGood manufacturing practices for pharmaceuticals :
_ba plan for total quality control /
_cSidney H. Willig and James R. Stoker
260 _aNew York :
_bMarcel Dekker, Inc.,
_cc1992
300 _aiii, 268 pages ;
_c23 cm.
504 _aIncludes bibliographical references and index.
505 _aStatus and Applicability of Regulations: Current Good Manufacturing Practices in Manufacturing, Processing, Packaging, and Holding of Drugs -- Finished Pharmaceuticals: General Provisions (Subpart A) -- Organization and Personnel: (Subpart B) -- Building and Facilities: (Subpart C) -- Equipment: (Subpart D) -- Control of Components and Drug Product Containers and Closures: (Subpart E)
650 _aPHARMACEUTICAL INDUSTRY -- QUALITY CONTROL
700 _aStoker, James R.
_eco-author
942 _2lcc
_cBK
999 _c6246
_d6246