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”Why do I have to notify both attributes 'Verifizierung im Pflichtbetrieb ab Hochladedatum' and 'Verifizierung im Pflichtbetrieb ab Verfalldatum' to IFA GmbH? | The attributes Verifizierung im Pflichtbetrieb ab Hochladedatum and Verifizierung im Pflichtbetrieb ab“ ... more
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”Which attributes must be notified to IFA GmbH regarding the implemented FMD on medicinal products obliged to verification and from what point in time is it possible to do so? | Both attributes Verifizierung im Pflichtbetrieb ab Hochladedatum and Verifizierung im“ ... more
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”What do the abbreviations mean in connection with the distribution channels? | The following abbreviations are used in the IFA documentation with the channels of distribution information: KVA / Krankenh.Apo. // VWeg KVA – distribution to hospital“ ... more
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”Does the supplier need to notify the Battery registration number by stiftung ear to IFA? | Please notify your product’s Battery registration number by stiftung ear for publication in the IFA database if the following applies: You are supplier of a product with a“ ... more
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”How can I notify product-specific address data for already published PZN? | There are two options for the notification of product-specific address data: Complete the address data (address number or company name of the marketing authorisation holder / local“ ... more
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”What is UDI? | UDI (Unique Device Identification) is a system to uniquely identify medical devices worldwide according to Article 27 of the MDR (Regulation (EU) 2017/745 dated 05.04.2017). UDI is the broader term for a unique product identification consisting of the“ ... more
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”Where can I find information on the anti-tampering device? | The anti-tampering decive, preventing interferance with the product, makes the first opening of the pack evident. Further information on the different options can be found on the website of the Deutsches“ ... more
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”What is NGDA? | NGDA (Netzgesellschaft Deutscher Apotheker mbH) runs the pharmacy server aiding pharmacists and other market participants medicinal products' verification. Scanning each pack before its dispense verifies the authenticity of the pack through data“ ... more
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”May I omit the PZN in Code 39 on the outer pack upon changing to the Data Matrix Code? | Pharmaceutical entrepreneurs are obliged to affix PZN in clear print and Code 39 or as Data Matrix Code (DMC) on the outer pack according to the amended frame agreement § 131 SGB“ ... more
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”What is the purpose of the attribute WEEE-Reg.-Nr. DE in the IFA Database? | Participants of the pharmaceutical market can gather information from the attribute WEEE-Reg.-Nr. DE (Registry number of stiftung ear according to ElektroG) such as the number itself under which“ ... more
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