Finished Pharmaceutical Products Quality Control (QC) Testing
Project Description
MULTIPLE PRODUCTS
MULTIPLE TESTING
ISO 17025 Africa Pharmaceutical Laboratory needed for quality control testing of various finished pharmaceutical products. Please respond with the following.
1 Schedule of Requirement (ToR)
2 RFQ Pricing Forms
Return completed offer forms with relevant technical and regulatory requirements, past experience and quality conformance related documents.
Required Accreditation and Certification for QC/Testing Laboratory
The Contracted QC laboratory must meet the following criteria in full:
1. Must be an ISO17025:2017 Certified for the required QC testing scope
2. Have the technical capability to adopt the in-house specifications for testing as provided by the manufacturer for non-compendia products.
3. Should be in a position to perform the method transfer process to validate the in-house method provided by the manufacturer.
4. Should be adequately equipped with appropriate equipment and should have the technical capabilities including well-qualified and trained staff to undertake the quality control on products required for testing.
5. Should be capable of communicating with the manufacturer (where required/permitted by UNOPS) in case samples are found to be out-of-specifications, to take decision to declare the products as non-compliant and advice on actions to be taken.
Required Document
Contracted QC Laboratory is required to provide the following documents with the quotation submitted.
- Valid ISO17025:2017 certificate with Testing/analysis scope
- Latest laboratory quality management audit report.
Project Information
Number:24-00733
Industry:Pharmaceuticals