000			01648cam a22004574a 4500
999			_c8437 _d8437
001			85332635
003			OCoLC
005			20190128092400.0
008			070112s2007 enk l 001 0 eng
020			_a9780853697190 (pbk.)
020			_a0853697191 (pbk.)
035			_a(OCoLC)85332635
040			_aNLM _cNLM _dEQO _dBAKER _dYDXCP _dOCLCQ _dFIN
042			_apcc
043			_ae------ _ae-uk---
060	0	0	_a2007 E-762
060	1	0	_aQV 33 FA1 _bR935 2007
082			_a615.19
090			_aRS141.3 _b.R8 2007
100			_aMHRA
245	0	0	_aRules and guidance for pharmaceutical manufacturers and distributors 2007 / _ccompiled by the Inspection and Standards Division of the Medicines and Healthcare products Regulatory Agency.
250			_aRevised edition
260			_aLondon ; _aChicago : _bPharmaceutical Press, _c2007.
300			_axviii, 430 p. ; _c25 cm.
650	1	2	_aLegislation, Drug.
650	2	2	_aDrug Compounding _xstandards.
650	2	2	_aDrug Industry.
650	2	2	_aPharmaceutical Preparations _xstandards.
650	2	2	_aQuality Control.
650		0	_aDrugs _xLaw and legislation _zEuropean Economic Community countries.
650		0	_aDrugs _xLaw and legislation _zGreat Britain.
650		0	_aPharmacy _xLaw and legislation _zEuropean Economic Community countries.
650		0	_aPharmacy _xLaw and legislation _zGreat Britain.
651		2	_aEurope.
651		2	_aUnited Kingdom.
655		2	_aGuideline.
655		2	_aLegislation.
710	1		_aGreat Britain. _bMedicines and Healthcare products Regulatory Agency. _bInspection and Standards Division.
942			_2ddc _cBK