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ComplianceOnline Home > ComplianceOnline Store > FDA Audit, Validation & Documentation – Checklist, Templates& master plans
 
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FDA Audit, Validation & Documentation: Quality & Compliance Manuals, Checklists & more - ComplianceOnline.com

FDA Audit, Validation & Documentation

ComplianceOnline is the largest resource on the web for latest checklists, templates, SOPs, master plans, procedures and application on standards and regulations across industries (FDA, SOX, ISO ,Medical Device, Pharma, Manufacturing, Construction, Environment, hitech).
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Featured Products
 
 
Design and Development-Reviews
The purpose of this procedure is to establish a planned system of reviews for Design and Development and to control the required revisions for verification and validation.
Provider: Quality Rite
Shipping: Available for download - Link will be provided in My ComplianceOnline section
Price: $25.00
Design and Development-Changes
The purpose of this procedure is to establish a system of controlling Design and Development changes after a product has been released for production.
Provider: Quality Rite
Shipping: Available for download - Link will be provided in My ComplianceOnline section
Price: $25.00
Purchasing
This procedure defines the system for ensuring that all purchased product conforms to specified requirements.
Provider: Quality Rite
Shipping: Available for download - Link will be provided in My ComplianceOnline section
Price: $31.00
View Sample Pages
Inventory Control
This procedure defines the system to control inventory using a bin [KanBan] system.
Provider: Quality Rite
Shipping: Available for download - Link will be provided in My ComplianceOnline section
Price: $25.00
Test Status
This procedure defines the method used to control the Test Status of product and materials at a company.
Provider: Quality Rite
Shipping: Available for download - Link will be provided in My ComplianceOnline section
Price: $21.00
 
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Featured Online Training
 
  Introduction to FDA Good Documentation Practices  
Instructor: Chris Whalley
 
This FDA Good Documentation Practices training will introduce and explain the concept of Good Documentation Practices, and provide real-world examples of how to, and how not to, use GDPs.  
  Introduction to FDA Good Documentation Practices  
Instructor: Chris Whalley
 
This FDA Good Documentation Practices training will introduce and explain the concept of Good Documentation Practices, and provide real-world examples of how to, and how not to, use GDPs.  
  Risk Assessment-Compliance Using Easy To Fill Out Documentation  
Instructor: David Nettleton
 
Learn how to perform risk assessment as part of the risk-based approach to computer system validation.