000			02083nam a22003615i 4500
001			310022
003			MX-SnUAN
005			20160429160337.0
007			cr nn 008mamaa
008			150903s2009 sz | o |||| 0|eng d
020			_a9783764383626 _99783764383626
024	7		_a10.1007/9783764383626 _2doi
035			_avtls000362887
039		9	_a201509030650 _bVLOAD _c201405070335 _dVLOAD _y201402211134 _zstaff
040			_aMX-SnUAN _bspa _cMX-SnUAN _erda
050		4	_aRM1-950
100	1		_aWood, Linda Fossati. _eeditor. _9350563
245	1	0	_aTargeted Regulatory Writing Techniques: Clinical Documents for Drugs and Biologics / _cedited by Linda Fossati Wood, MaryAnn Foote.
264		1	_aBasel : _bBirkhäuser Basel, _c2009.
300			_brecurso en línea.
336			_atexto _btxt _2rdacontent
337			_acomputadora _bc _2rdamedia
338			_arecurso en línea _bcr _2rdacarrier
347			_aarchivo de texto _bPDF _2rda
500			_aSpringer eBooks
505	0		_aRegulatory writing fundamentals -- Developing a target -- Getting started -- Regulatory writing tips -- Templates and style guides: The nuts and bolts of regulatory documents -- Document review -- Source documents -- Protocols -- Clinical study reports -- Integrated documents -- Investigator’s brochures -- Investigational medicinal products dossier -- Integrated summaries of safety and efficacy -- Informed consent forms -- Regulatory submissions -- Global submissions: The common technical document -- Clinical trial procedures and approval processes in Japan -- Region-specific submissions: United States of America.
590			_aPara consulta fuera de la UANL se requiere clave de acceso remoto.
700	1		_aFoote, MaryAnn. _eeditor. _9325141
710	2		_aSpringerLink (Servicio en línea) _9299170
776	0	8	_iEdición impresa: _z9783764383619
856	4	0	_uhttp://remoto.dgb.uanl.mx/login?url=http://dx.doi.org/10.1007/978-3-7643-8362-6 _zConectar a Springer E-Books (Para consulta externa se requiere previa autentificación en Biblioteca Digital UANL)
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999			_c310022 _d310022