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ISO 13485 2016 documents contain more than 100 editable MS-Word files. These editable documents address all the elements of the medical device quality management system. The entire iso 13485 documents are written in easy-to-understand language. As well as the Hand-outs are managed in MS Word documents. The soft copy of the documentation kit and audit iso 13485 checklists also form a part of this kit. The downloadable DEMO is available, which guides users and ISO 13485 consultants to understand the content of documentation included in the product.
ISO 13485 Manual and other quality system documents are developed under the guidance of experienced quality experts. The kit is designed to save much of your time in typing and preparing a presentation as well as documentation. It is user-friendly and easy to learn. The set of ISO 13485 documents defines the baseline system with ISO 13485 audit checklist that satisfies standard requirements, which can be customized to suit your requirements. It provides a model of quality system documentation that is natural, simple, and free from excessive paperwork. To know more, visit here: https://www.documentationconsultancy.com/iso-13485-documents.html
ISO 13485, published in 1996, requires a comprehensive quality management system for medical device design and manufacturing. To achieve ISO 13485 cer...
Global Manager Group provides ISO 13485 Medical Devices QMS Documents in editable format. The ISO 13485 documents contain more than 100 editable MS Wo...
ISO 13485 2016 documents contain more than 100 editable MS-Word files. These editable documents address all the elements of the medical device quality...
ISO 13485 certification consultancy and total documentation for quality management system of companies involved in design, manufacture, supply and ser...
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