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”To which date can I terminate my contract with IFA GmbH? | IFA's supplier contract may be terminated by either side with a time limit of three months to the end of each calendar year in written form to the other partner: form for termination of the IFA supplier“ ... more
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”May packs not bearing security features still be dispensed after 09.02.2019? | Yes, if it is actual Bestandsware released to the market prior to the 09.02.2019. For the systems to identify these packs as Bestandsware, the pharmaceutical entrepreneur must notify the“ ... more
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”Here you will find notification order files guidelines contract documents and further information of IFA GmbH availale for download Please note Some IFA documents are only available in German“ more
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”Who assigns the UDI-PI? | The manufacturer assigns the UDI-PI in accordance with the requirements of the MDR regarding traceability (cf. IFA Specification UDI).“ more
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”Who assigns the UDI-DI? | The manufacturer has to contact one of the issuing entities named by the European Commission. IFA GmbH is one of these issuing entities. “ more
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”How can I report a UDI-DI to the IFA? | IFA GmbH has implemented a data field in which to report an UDI-DI. The UDI-DI of a different issuing entity can also be entered there.“ more
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”Unique Device Identifier (UDI) | Technical Information on PZN Coding -Check Digit Calculations- (225 KB) more
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”Unique Device Identifier (UDI) | Specification UDI Use of the IFA Coding System for MD (1,5 MB) 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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”Where can I find further information on implementing the FMD in the IFA database? | Information on implementing the Falsified Medicines Directive 2011/62/EU (FMD) and its Delegated Regulation (EU) 2016/161 (dVO) in the IFA database can be found in Guidelines for Notifying“ ... more