The alert message may indicate an attempt at counterfeiting and is automatically forwarded to the competent authorities.
The batch number entered could not be found. Possible reasons:
The pack must be separated and must not be brought to market until the cause of the alert has been determined.
In most cases, this message indicates that an incorrect entry has been made (possibly a manual entry). Please check first that all the details have been entered correctly. Compare the scanned data with the details printed in plain text on the pack.
PLEASE NOTE! A pack with a code error is not fit for sale. Every subsequent link in the pharmaceutical supply chain will receive the same error message and refuse your delivery.
Special case returns: If a parcel is returned, the person in charge may apply simplified quarantine rules, for example by authorising the parcel to be destroyed immediately. The parcel may have been returned because it was unfit for distribution.
Special case brand-new medicines: It cannot be ruled out that packs may already have been dispatched to the 3PL, even though the relevant data has not yet been uploaded to the verification system. Please contact the manufacturer to clarify such cases directly.
Our support team is always there for you.
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Please allow up to 24 hours for your order to be processed. We will then send the newly generated Aggregation Codes as a PDF to the email address provided here.
Is your FMD Speed Scanner no longer working? To ensure you can continue working without interruption, we will send you a replacement device as quickly as possible. At the same time, you will receive a return label for sending back your defective device.
You will receive the replacement unit regardless of whether your warranty is still valid.
Do you suspect counterfeiting? Our medAspis Alert Team will assist you with the process. We are also happy to assist you with unclear error messages or unfamiliar situations.
Describe the incident using the report form. If needed, you can upload up to three photos. We will contact you as soon as possible and support you with the next steps.
Companies in the pharmaceutical industry are validated and meet strict quality requirements. Nevertheless, there is still a significant compliance risk with FMD.
Suspected falsification cases may not be handled and documented in a GxP-compliant manner.
With our free, anonymous and non-binding Compliance Check-up, we analyse and assess your company’s critical FMD error messages.
Based on your existing FMD audit trails, we analyse among other things:
The analysis is performed entirely within your data system. No data is transmitted to medAspis. All evaluations remain anonymous.
Download the error messages directly to your computer in your local language.
Can’t find your language? As soon as you become a customer, we’ll of course provide the error messages in your local language. Promise.
medAspis stands for proven quality and traceable processes. Lean FMD provides the necessary framework for this.
Lean FMD is validated in accordance with EU-GMP Annex 15. medAspis operates a Quality Management System in accordance with ISO 9001 and supports you with validation and the required documentation.
With the Validation Toolkit, you receive the documentation for the validation of Lean FMD. This enables you to carry out the necessary validation steps in a structured and traceable manner.
Download an excerpt from the Validation Toolkit to get a first impression of the structure and process of validation.
The complete toolkit contains all the necessary documents for validating Lean FMD.