ComplianceOnline
Best Practices Best Practices
Online Training Online Training
Seminar Seminar
Standards
Welcome,
Guest
Free Registration | Sign In
ComplianceOnline Home > ComplianceOnline Standards > FDA Audit, Validation & Documentation – Checklist, Templates& master plans
 
 Browse Category
 
    Aerospace
    Agriculture and Farm Machinery
    Automotive, Aircraft & Marine technology
    Banking, Corp. finance & Sox
    Biotech & Pharmaceutical Standards
    Chemical technology
    Civil engineering and construction
    Computer Hardware
    Electrical Engineering
    Electronic Equipment
    Energy and Heat Transfer Engineering
    Environment & Health protection
    FDA Audit, Validation & Documentation
    Food Technology
    GXP Compliance Tools New
    HIPAA Compliance
    Human Resource
    Industry Reports New
    ISO Published Standards
    IT and PCI Compliance
    Leather and Textile
    Manufacturing Engineering
    Medical Device and Healthcare Technology
    Metal, Mining and Minerals
    Packaging and Distribution
    Paper and Plastic Industries
    Petroleum products
    Quality Terminologies & Documentations
    Safety Engineering
    Test Methods & Procedures
    Trade Supply Chain and Logistics
 
Describes procedures for generation, distribution and maintenance of SOPs as required by the regulated healthcare industry and by organizations that should comply with quality or accreditation standards such as ISO 9000 or 17025 standards.
Author: Dr. Ludwig Huber
Shipping: Available for download - Link will be provided in My ComplianceOnline section
Source: LabCompliance
Price: $49.00

Product Detail:
  • Describes responsibilities and procedures to initiate new SOPs.
  • How to develop and distribute SOPs?.
  • How users should be trained and how SOPs should be audited and updated?.
  • The SOP also includes three attachments with templates and a complete list with content requirements for easy implementation.

Scope of Product:

The SOP applies to operations in GXP regulated environments and to organizations that should comply with quality or accreditation standards such as ISO 9000 series or 17025.

Who will benefit:

  • Staff in Operations
  • Operations Supervisors
  • Documentation Department
  • Quality Assurance Department
Customer Testimonials
This product hasn't been reviewed yet.
Review this product
 
 Member Service
 
Toll Free  +1-888-717-2436
Fax  +1-650-963-2556
Email  editor@complianceonline.com
 
 Your Shopping Cart
Contains 0 items    Total: $0.00
Customers Also Bought
Quality System Flowchart
Price: $9
 
Quality Control Policy
Price: $97
 
Validation of Tools and Molds
Price: $27
 
Validation Plan
Price: $97
 
Warranty Product Review
Price: $9
 
Writing Procedure-1
Price: $37
 
Related Trainings
Maintaining an Effective CAPA Program and Using Risk Assessment Tools: Current T...
 
Practical tips to comply and implement the Adverse Event Reporting requirement o...
 
Change Management for Regulated IT Processes
 
Challenges for the RA Professional, and How to Address Them