This system is used in Austria, Belgium, Cyprus, Estonia, Finland, France, Hungary, Latvia, Luxembourg, Malta, the Netherlands, Norway, Poland, Portugal, Romania, Slovenia, Spain and the United Kingdom (Northern Ireland).
Before this process step can be performed, the user has to be registered with his responsible NMVS and received the access data to be entered here. First, all user data is entered and then the username and initial password received from the NMVO are entered in the “Certificate” section.
The certificate is then downloaded. First, the certificate window must be opened by clicking the “plus” symbol.
The certificate file (p.12) previously provided by the NMVO is uploaded and the certificate password and password token are entered. Both data are provided by the NMVS. The certificate window is closed with OK and the entire process is completed with “Save”.
Afterwards, the Arvato Terms and Conditions are confirmed in the Arvato main window and the initial password is changed. Buttons are available for both processes in the upper part of the window.
The new password is confirmed with OK. The password window closes.
The process is completed, the system is connected to the responsible NMVS.
Continue to the next step: Registering users at the Speed Scanner >
Our support team is always there for you.
Please use a larger screen to view the full support menu.
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.