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ISO 9001:2008
ISO/TS 16949:2009
Software Engineering
FDA Checklist-Kit for
Medical Device Firms
FDA Requirement
ANSI/AAMI/ISO 13485:2003 Requirements Checklist
ANSI/UL 1998:2004 Checklist
IEC 60601-1-4 Checklist
IEC 62304:2006 Checklist
ISO/IEC 90003:2004 Supplier Assessment
ISO 9001:2008 Evidence Product Checklist
FDA Guide, Pre-market Submissions, Software in Medical Devices
FDA Software Validation Checklist
FDA Off-the-Shelf Software in Medical Devices, Checklist
Templates for Software and System Management
Guides to
Software Engineering
Standards
Reference
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ISO 9001:2008
ISO/TS 16949:2009
Software Engineering
FDA Checklist-Kit for
Medical Device Firms
FDA Requirement
ANSI/AAMI/ISO 13485:2003 Requirements Checklist
ANSI/UL 1998:2004 Checklist
IEC 60601-1-4 Checklist
IEC 62304:2006 Checklist
ISO/IEC 90003:2004 Supplier Assessment
ISO 9001:2008 Evidence Product Checklist
FDA Guide, Pre-market Submissions, Software in Medical Devices
FDA Software Validation Checklist
FDA Off-the-Shelf Software in Medical Devices, Checklist
Templates for Software and System Management
Guides to
Software Engineering
Standards
Reference
Services
Publishing
Translations
Consulting
Quality Management Systems and Software Engineering
Products and Services
ISO 9001 and ISO / TS 16949 Quality Management Systems
For
Software Engineering Standards - Templates - Guides - Checklists
IEC 60601-1-4,
FDA 21 CFR, ANSI/AAMI/ISO 13485, ANSI/UL 1998, ANSI/AAMI SW68,
ISO/IEC 90003,
IEC 62304,
ISO/IEC 15288,
ISO/IEC 27002, ISO/IEC 20000-1, ISO 9001, ISO/IEC 12207,
ISO 90003
Publishing, Books, CD-ROMs, Software
Business - Management Consulting, ISO 9001, ISO/TS 16949
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/ Spanish > English
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español > inglés / inglés > español
ISO 9001:2008
for
Manufacturing Industries
FDA Checklist Kit
for Medical Device Firms
for requirements of
ANSI/AAMI/ISO 13485:2003, ANSI/UL 1998:2004,
IEC 60601-1-4, IEC 62304:2006, ISO 9001, ISO/IEC 90003
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Thursday 29 July, 2010
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