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Contract testing laboratory - quality questionnaire
Quality Contracts
Description:
This ready-to-use quality audit questionnaire (audit by mail) has been created to assess potential contract laboratories, to test their quality standards and regulatory profile and reassure your company that the contract laboratory is able to operate in line with current good manufacturing/laboratory practices. The questionnaire also includes a covering letter, which only needs a small amount of site-specific modification before it can be used.
During on-site audit preparation work, this checklist can be used to draw up the audit agenda and help with the execution of a systematic on-site GMP audit. Please remember that as long as your company name is on the product to be tested, you are legally responsible for ensuring that the product tests carried out on your behalf meet all quality specifications and comply with all legal regulatory requirements imposed on testing.
Download sample page
Price:
199.– EUR
*
(appr. 257.- USD)
* additional 19% tax for customers from germany / no shipping costs will be charged
Delivery item:
Open Word Document
You will be able to enter your data into the Word document.
Please note: We do not deliver hard copies.
Further details:
Table of content
1 Document Request.
2 Quality Organization
2.1 General Information
2.2 Key Personnel
3 Regulatory and Quality Profile
3.1 Laboratory Registrations / Accreditations
3.1.1 Registrations
3.1.2 Accreditations
3.1.3 Quality Management Systems
3.2 Governmental Inspections / Governmental Relations
3.2.1 Good manufacturing Practices (GMPs)
3.2.2 Critical Health authority occurrences
3.3 Sub contracting and conflict of interest
3.3.1 Conflict of interest
3.3.2 Sub contracting
4 Quality Systems
4.1 Equipment Inventory
4.2 Analytical Testing
4.2.1 QC laboratory water
4.2.2 Expiry dates of solutions
4.2.3 Method validation
4.2.4 Standards
4.3 Out Of Specification (OOS) Results
4.4 Retention Samples / Reserve Samples
4.5 Documentation
4.6 Training
4.7 Stability
4.8 Computer Operations and 21CFR Part 11
5 Response Approval
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