Printinspection for Pharmaceutical Companies

The EyeC Proofiler is designed to identify systematic errors between the Signed-off proof and the printed samples. Identifying these systematic errors is important in any application but for GMP companies it is crucial. Any errors in information provided to patients, e.g. wrong or missing text on patient information leaflets, cartons or labels, exposes pharmaceutical companies to a risk of litigation and a damaged reputation.

With this in mind, EyeC does not only offer a qualified product, for print inspection but we support our pharmaceutical clients during the validation phase by offering relevant documentation including a Functional Requirements Specification (FRS), Installation Qualification(IQ) and Operational Qualification (OQ) , The OQ includes a validation card which can also be used for ongoing periodic validation checks of the system. All EyeC products are fully compliant with GAMP4 and 21 CFR part 11.

Eliminating human/operational errors is essential to ensure a smooth and lean inspection process by reducing the inspection time and increasing quality. Hence, the Proofiler offers an intuitive approach and is an easy-to-use product being seamlessly integrated in your quality process.