Curated News
By: NewsRamp Editorial Staff
October 10, 2024

Documentationconsultancy.com Relaunches ISO 13485 Documents Toolkit for Medical Device Quality Management Systems

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Source News Release

TLDR

  • Gain a competitive advantage by quickly implementing a strong Medical Device Quality Management System (MDQMS) that complies with ISO 13485 standards.
  • The ISO 13485 Documentation Toolkit provides a full set of required and supplementary documents designed to meet ISO 13485:2016 criteria.
  • The documentation toolkit helps medical device manufacturers, design and development firms, and other organizations save time and money while ensuring ISO 13485 certification.
  • The ISO 13485 Documents Toolkit offers a collection of easily editable documents, including quality manual, procedures, exhibits, formats, SOPs, process flow charts, audit checklist, and medical device file.

Impact - Why it Matters

This news matters to businesses in regulated industries, particularly medical device manufacturers seeking ISO 13485 certification. The relaunched toolkit and consultancy services provide a comprehensive solution for system implementation and auditing, saving time and costs while ensuring compliance with ISO 13485 standards.

Summary

Documentationconsultancy.com has announced the relaunch of its valuable Editable ISO 13485 Documents Toolkit, designed for businesses seeking ISO 13485 certification for their medical device quality management systems. The toolkit includes a full set of required and supplementary documents, as well as online consultancy and support services for system installation and auditing. This resource is a valuable asset for various organizations, including medical device manufacturers, contract manufacturers, design firms, and companies transitioning from previous ISO 13485 versions.

Source Statement

This curated news summary relied on this press release disributed by 24-7 Press Release. Read the source press release here, Documentationconsultancy.com Relaunches ISO 13485 Documents Toolkit for Medical Device Quality Management Systems

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