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BS EN ISO 13485:2016 - TC

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Tracked Changes. Medical devices. Quality management systems. Requirements for regulatory purposes
More Information
ISBN9780539038224
Publication StatusCurrent
Publication Date21/02/2019
Format (Paperback, Hardback etc)PDF (Electronic delivery via Email)
Total Pages179
Brand / PublisherBSI
PublisherBSI

Official BSI Distributor

What is a tracked changes standard?

A tracked changes version of a Standard indicates the changes made, during the standards revision process, between the active standard and its previous version. Additions, deletions, and other formatting and/or content revisions are clearly displayed as underlined and strikethrough texts, ensuring all changes made between the two documents are quickly and easily identified.

What is this standard about?

This International Standard specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. Such organizations can be involved in one or more stages of the life-cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device and design and development or provision of associated activities (e.g. technical support). This International Standard can also be used by suppliers or external parties that provide product, including quality management system-related services to such organizations.

Requirements of this International Standard are applicable to organizations regardless of their size and regardless of their type except where explicitly stated. Wherever requirements are specified as applying to medical devices, the requirements apply equally to associated services as supplied by the organization.

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