Your Shopping Cart
VALIDATION POLICY
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
- This policy applies to all items requiring validation, including facilities, utilities, equipment, processes, quality control methods, and computerized systems that could potentially impact the purity, potency, or quality of a product, or are used for GxP functions , and/or to generate, store, manipulate or retrieve electronic quality records.
- Policy is also stated for the purpose of validation, requirements of the validation process, the use of validated systems, retention of validation records, and supplier adherence to the policy.
- This document is best used by companies that use computer systems throughout the product life cycle , i.e., from research through production.
It Provides information on:
- Responsibilities.
- Method.
- Quality records.
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: $167 BUY NOW - ISO 13485:2016 “Medical Devices - Quality Management Systems- Requirements for Regulatory Purposes”
Price: $330 BUY NOW - Evidence Product Checklist For UL 1998 Standard for Safety - Software in Programmable Components
Price: $330 BUY NOW - IEC 62304:2015 ''Medical Device Software - Software Life Cycle Processes''
Price: $167 BUY NOW - Checklist for FDA, Guidance for the Content of Pre-market Submissions for Software Contained in Medical Devices.
Price: $167 BUY NOW - FDA, General Principles of Software Validation Final Guidance for Industry and FDA Staff (Release date January 11, 2002)
Price: $330 BUY NOW
You Recently Viewed