Validation Master Plan Template
Provider: BPA
Shipping: Available for download - Link will be provided in My ComplianceOnline section
Shipping: Available for download - Link will be provided in My ComplianceOnline section
Price:
$99.00
Product Details
- Companies who have a number of computer systems and are just starting to validate them need to determine what really needs to be validated and the priorities for the validation.
- This template describes the information that needs to be presented in a validation master plan and provides examples. 9 pages
- The Validation Master Plan is a high level plan that identifies all the computerized business systems at a site (or for an organizational unit) that require validation, sets priorities based on defined criteria, and states time frames for such validations.
It Provides information on:
- Organization
- Systems
- Validation Plan and Timeline
Customers Also Bought
- 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 Cyber security for Networked Medical Devices Containing Off-the Shelf (OTS) Software"
Price: $330 BUY NOW - Checklist for FDA, Guidance for the Content of Pre-market Submissions for Software Contained in Medical Devices.
Price: $330 BUY NOW - Electronic Signatures; Final Rule-FDA 21CFR Part 11
Price: $167 BUY NOW - FDA, General Principles of Software Validation Final Guidance for Industry and FDA Staff (Release date January 11, 2002)
Price: $167 BUY NOW - ISO 13485:2016 “Medical Devices - Quality Management Systems- Requirements for Regulatory Purposes”
Price: $167 BUY NOW - Evidence Product Checklist For UL 1998 Standard for Safety - Software in Programmable Components
Price: $167 BUY NOW
You Recently Viewed
