000 01332cam a2200313 a 4500
005 20250914135702.0
008 050322s1998 xxu b 001 0 eng
010 _a98-010632
020 _a087389426X (alk. paper)
_cRM657.93
039 9 _a200506031706
_bwahab
_c200505251600
_drapiza
_y03-22-2005
_zrazalis
090 _aKF3827.M4.K893 1998
090 0 0 _aKF3827
100 1 _aKuwahara, Steven S.
245 1 0 _aQuality systems and GMP regulations for device manufacturers :
_ba practical guide to U.S., European, and ISO requirements /
_cSteven S. Kuwahara
260 _aMilwaukee, Wis. :
_bASQ Quality Press ;
_aBuffalo Grove, Ill. :
_bInterpharm Press ,
_c1998
300 _axviii, 236 p. ;
_c24 cm.
504 _aIncludes bibliographical references (p. 213-215) and index
650 0 _aMedical instruments and apparatus
_xStandards
_zUnited States
650 0 _aMedical instruments and apparatus
_xStandards
_zEurope
650 0 _aMedical instruments and apparatus industry
_xLaw and legislation
_zUnited States
653 0 _aCurrent Good manufacturing practices (CGMP)
907 _a.b13497479
_b2021-05-28
_c2019-11-12
942 _c01
_n0
_kKF3827.M4.K893 1998
914 _avtls003302051
990 _azaa
991 _aJabatan Farmasi, KKL
998 _ad
_b2005-09-03
_cm
_da
_feng
_gxxu
_y0
_z.b13497479
999 _c348962
_d348962