
eyetec is a trusted partner for healthcare industries
With more than twenty years’ experience in technical pharmaceutical manufacturing, eyetec perfectly understands the challenges companies in the pharmaceutical industry, hospitals and pharmacies face.
our services
eyetec is a leading international expert in visual inspection and container closure integrity testing (CCIT). In addition, eyetec provides a vast array of services for the healthcare sector. These include sales, design, maintenance, calibration, and qualification support of pharmaceutical manufacturing equipment.
eyetec is renowned for visual inspection and CCIT, ensuring compliance, technical and operational efficiency of the production process of parenteral pharmaceutical products.
                    test samples
                    consultancy
                    vision engineering
                pharma equipment
eyetec is the official Benelux distributor and after-sales partner for several high-quality pharmaceutical machine brands.
                    equipment sales
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                    after-sales support
                qp and qa services
eyetec offers QP services mainly for the ATMP and biotech sectors. We can also act as interim QA manager or follow up on limited assignments.
                    qp and qa services
                in the spotlight
Visual Inspection & CCIT
                            Getting Automated Visual Inspection right from the start
Bram Keymolen speaking at PDA APAC 2025, Incheon, Korea
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                        jobs
                            Project Engineer
We are looking for a motivated Project Engineer to join our growing team.
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                        Visual Inspection & CCIT
                            Visual Inspection Training for compliant and consistent inspection
eyetec’s Manual Visual Inspection Training Days (2–3 December 2025, Radisson Park Inn Brussels Airport) deliver a focused, English-language program that connects EU and US compliance expectations with real-world inspection performance. 
Across two days, participants combine regulatory understanding, case studies and hands-on exercises using real defect samples to strengthen process reliability, operator skill and audit readiness.
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            A unique combination of production, engineering, and compliance expertise.
Because of its combined experience in both compliance as well as technical aspects of pharmaceutical manufacturing, backed up by more than twenty years of experience in GMP manufacturing.
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