Have you counted your cost to comply with the Falsified Medicines Directive?

Upwards of $1.77 can be added to the cost per drug package as a result of the high levels of investment needed to comply with the Falsified Medicines Directive (FMD)*

Ci-DMS MES is configured and validated for compliance, electronic records and processes improve data integrity whilst reducing our customers’ overheads associated with maintaining compliance.

In most cases, a return on investment is achieved within one year.

*source: Capgemini Consulting

Ci-DMS MES in the Packing Suite

All significant operator actions can be configured to require an electronic signature

Ci-DMS MES Packing

Reduce your cycle times

Remote approvals can be configured as required on completion of an operation (e.g. equipment validation) or stage (e.g. granulation).

Approval must be given before production can continue.

On completion of an order, information can be reviewed in its entirety or by exception prior to release.

Ci-DMS MES in action

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Solve modern industry challenges with CI Precision

From our industry-leading precision weight sorters to advanced MES solutions, our products and services have been engineered to help you address and overcome your unique industry challenges.


Download the Ci-DMS MES brochure

Learn more about our Ci-DMS MES — our powerful, versatile, and modular software for paperless manufacturing that helps you tackle even the most exacting and demanding production requirements.


Automated, high-precision weight sorting for superior quality control

When Harwell Dosimeters wanted to control the manufacturing quality of their Alanine Pellets they chose CI Precision’s weight sorters to accurately weigh each pellet.

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