C33 PlusLine Pharma Checkweigher

Compliance-supporting Software Options

Software options such as Local Audit Trail and Login Server along with individual user profiles with password protection support regulatory FDA 21 CFR Part 11 compliance by recording all implemented changes and providing data integrity for audit purposes.

Effective Process Optimization

Avoiding line jams and stoppages is essential for maximizing uptime. Effective product handling solutions such as side grips and top and bottom belts combined with effective reject mechanisms result in minimal false rejects for optimum efficiency.

Modular, Flexible, Future-proof Design

The space-saving modular system architecture supports future modifications. Process data is clearly displayed on a 12" high-contrast touchscreen offering intuitive use in over 30 languages.

Reliable Accuracy

Robust strain gage or digital monoblock electromagnetic force restoration (EMFR) load cells achieve reliable precision for lightweight products. Intelligent filter algorithms eliminate vibrations from the environment and calculate the mean weight.

Testing and Documentation for Compliance

The Equipment Qualification (EQ) Pack offers complete equipment qualification covering procedure description, DQ/IQ checklists and OQ tests. It also includes protocols, diagrams and certificates to ensure compliance with FDA and GMP regulations.

Simple Production Line Integration

Tailor the checkweigher to your production needs with integration options, including networking for multiple checkweighers, communication interfaces and optional line monitoring systems.

Global Service Support

A global network of service experts provide fast remote and on-site support. Our comprehensive service offer allows you to achieve regulatory compliance, high performance, and maximum uptime throughout the life cycle of your product inspection equipment.