Describes procedures for equipment qualification 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 –
Write specifications.
Qualification of the vendor.
Installation.
Development.
Contents of system inventory.
Testing prior to use (operational qualification) and for on-going testing (performance qualification).
The SOP also includes four attachments with templates for easy implementation.
Purpose:
Documented qualification of equipment throughout the entire cycle: comparing user
specification with vendor specification, vendor qualification, installation, initial and
ongoing testing.
If there is a specific reason, alternative scientifically based approaches may be
used. The use of alternative approaches should be justified, documented and
approved and should comply with applicable GxP regulations and company
standards.