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The experts at SEPT have updated Guidance for Industry, FDA Reviewers and Compliance on Off-the-Shelf Software Use in Medical Devices to reflect the suggested compliance with the document Compliance on Cyersecurity for Networked Medical Devices Containing Off-the Shelf (OTS) Software dated January 14, 2005.
This checklist reflects these new requirements. The Checklist provides an easy-to-use classification scheme of physical evidence comprised of procedures, plans, records, documents, audits, and reviews. The Checklist clarifies what is required for compliance through a product evidence list that will assist any software organization in meeting the requirements of this guideline.
Use of the Checklist will save time and money, and may aid in meeting certain governmental requirements.
A quality product at a reasonable price!
Document identifier
SEPT FDA Guidance Checklist
Title
Checklist for the FDA Document Guidance for Industry, FDA Reviewers and Compliance on Off-The-Shelf Software Use in Medical Devices? As Amended by ?Guidance for Industry, FDA Reviewers and Compliance on Cyersecurity for Networked Medical Devices Containing Off-the Shelf (OTS) Software
SEPT Category
Medical Device Checklists
Publication date
2005-05-01
International Relationship
Price |
149 vnd |