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

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

Dispensing Suite

Granulation Suite

Packing Suite

How you can meet us

Request a meeting, or find us at an exhibition

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