Description
The custom QC process begins with the laboratory submitting their analyte requirements. UTAK returns a draft formulation specification within 48 hours. After agreement on concentration ranges and matrix type, the product is manufactured, QC-tested, and shipped with a complete documentation package including certificates of analysis, stability data, and traceability records. Successful formulations can be converted to stocked inventory for ongoing supply.
Key Details
- Turnaround: Approximately 15 working days from confirmed specification
- Draft formulation specification provided within 48 hours of enquiry
- Available in serum, urine, whole blood, oral fluid, and specialty matrices
- Full documentation package included with every lot
- Supports CAP, CLIA, and ISO 15189 compliance requirements
- Custom formulations can be converted to recurring stocked inventory
For a complete product listing, download the full UTAK QC Products Catalogue.
