Quality Control Systems for Pharmaceutical CompaniesQuality Control Systems for the Printing & Packaging Industry - EyeC

Pharma & Healthcare

Print inspection for pharmaceutical and healthcare packaging

A proven solution in the pharmaceutical industry, EyeC offers user-friendly and innovative artwork and print inspection systems. Our solutions help you perform efficient and dependable quality checks at each of the production stages and avoid product recalls.

With our file-to-file comparison software, control your files from the first artwork to the final pre-press file. With our print sample testing solutions, ensure the quality of your printed products before sending them to the production line.

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Reliable quality controls

The EyeC systems have been developed with a strong emphasis on reliability, speed and ease of use. They verify the quality of files or printed materials against one or several approved files. In addition to the inspection of text and graphics, EyeC offers several options such as the inspection of Braille, 1D and 2D codes or colors. Our systems detect all items automatically and inspect their complete content in one inspection cycle and in record time. All potential differences are pinpointed with great precision. At the end of the inspection, the systems deliver a comprehensive report.

Secure inspection processes

The EyeC Proofiler print sample testing solution meets the latest requirements of data integrity and safety, and provide an audit trail. The system increases the security of quality controls thanks to closed processes and a secure database. A dedicated pharmaceutical workflow makes it easy to integrate our inspection systems into existing processes. The EyeC Audit Trail Viewer allows an easy review of the audit trail based on customizable filters. By using our systems, you avoid product recalls, perform quick and automated quality controls, increase the security of your data and processes, and are well-prepared for audits.

Compliance to pharmaceutical guidelines

The EyeC software is produced in conformance to applicable ISO 9001, GMP, GAMP 5, and contains all functions necessary for a validation according to the guidelines laid out in U.S. FDA Title 21 CFR Part 11. In addition, we support our pharmaceutical clients during the validation phase by offering a complete validation support package including all validation-relevant documents such as URS, IQ, OQ, certification charts.

 

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