A document confirming the test results and the compliance of the product batch with the customer’s requirements and applicable legislation.
For manufacturers and suppliers of metal products, polymers, electrical equipment, foodstuffs, pharmaceuticals, and other goods when a client or regulator requires an official test report.
Valid for the specific batch; documentation is retained for at least 10 years (ISO 9001:2015, clause 8.6).
It is a certificate or test report confirming that the product meets the stated technical specifications. The format depends on the industry: EN 10204 Type 3.1 for steel, Certificate of Analysis (CoA) for chemicals, and GMP Batch Certificate for pharmaceuticals.
It includes the manufacturer’s details, batch/heat number, test methods, and results.
It is required by the buyer for acceptance, as well as for insurance and customs procedures.
It may be issued electronically with a qualified electronic signature and references to laboratory reports.
Alstera will organize testing, issue EN 10204 certificates, CoAs, or GMP Batch Certificates, and coordinate them with inspection bodies.
2.1 — declaration of conformity;
2.2 — test report (routine tests);
3.1 — inspection certificate signed by the manufacturer’s quality department;
3.2 — inspection certificate with an additional signature by an independent inspector.
Yes, provided they bear an electronic signature and allow traceability to the original laboratory data (ISO 17025, Regulation (EU) 2019/1020).
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