Consulting for the implementation of the FMD guidelines
As a participant of securPharm and EMVO (European Medicines Verification Organisation), EurimPharm Produktions GmbH already has many years of experience in implementing the guidelines. We have built up a network of partners that can guarantee the handling of a hardware and software project for implementation at the customer's site.
Together with a selected machine builder and serialisation specialist, we offer both the necessary validatable software and hardware for the customer. Professional and efficient project management is a matter of course.
For customers whose Rx pharmaceutical portfolio is limited or who have not realised their investment by the necessary implementation date, EurimPharm Produktions GmbH naturally offers the takeover of the secondary packaging including all required serialisation steps as a service at any time.
