As a pharmaceutical logistics company, the topic of FMD affects you directly. With Lean FMD‘s 3PL module, you can carry out and spped up all relevant FMD processes on behalf of the manufacturers.
The topic of serialisation plays a decisive role for process speed in the supply chain of medicinal products When tens of thousands of packages have to be reliably and officially scanned every day as part of the EU Falsification Directive, this means a considerable time and therefore also cost factor. And we think that has potential for savings.
medAspis has recognised the challenges of the logistics industry and developed a techno-logically advanced serialisation solution.
Lean FMD fulfils all the requirements that you, as a pharmaceutical logistics company, place on serialisation processes. And we even solve problems that you haven’t even thought of yet, so that you can always stay ahead of the competition.
Lean FMD provides you as a pharmaceutical logistics provider with the right solution for all logistical serialization processes relating to FMD.
Lean FMD is perfectly tailored to your needs as a pharmaceutical logistics provider. This means that our service also meets your high compliance and GDP requirements at the same time, in order to reduce risks and ensure quality. With the zero-alert strategy, there are virtually no more false alarms that are reported to the authorities. Only extremely few real suspected counterfeit cases remain. In these cases, we support you with our unique know-how and provide the right solution: from practical instructions for scanning staff to the professional handling of critical counterfeiting suspicions. Thus, there is no reason for the authorities to examine the issue of FMD more closely during the next audit.
As a pharmaceutical logistics company, you have a special advantage with Lean FMD: not only do the authorities receive fewer counterfeit alerts, but the manufacturers do too. So your customers. The fewer false alarms, the better. This is because the amount of false alarms can be seen as an indicator of lack of compliance. Because you bring alert messages to practically zero with medAspis, you show your customers that your logistics are quality-controlled.
Would you right now like to learn more about how Lean FMD can speed up your serialisation processes around FMD and make them safer? Just give us a call. We will be happy to advise you personally – even if you simply have a question about FMD and are not yet our customer.
» At three different locations, we move 1.2 billion pharmaceutical packages every year. Therefore, Lean FMD and its resulting efficiencies are perfect for us. The medAspis experts also accompanied us during the implementation according to GxP guidelines on every single step. They responded flexibly and competently to our wishes and implemented them together with us. The FMD solution is now perfectly integrated into our own systems.
Our conclusion: medAspis is a strong partner in every respect. «
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.