Search

HomeFAQ

FAQ

”What happens if I do not notify the attributes for my medicinal products obliged to verification 'Verifizierung im Pflichtbetrieb ab Hochlade- / Verfalldatum'? | If the supplier fails to notify the attributes Verifizierung im Pflichtbetrieb ab Hochladedatum and“ ... more

HomeFAQ

FAQ

”What is a Generikaabschlag? | A Generikaabschlag (generics discount) is the manufacturer's discount according to § 130a paragraph 3b SGB V. Further information can be found in the consensus guideline between relevant manufacturers' associations and the“ ... more

HomeFAQ

FAQ

”What clear print requirements are there for German-Austrian multi market packs? | As for single market packs, the four elements of the unique identifier (UI) must be affixed in clear print adding the nationally predefined label. Please pay attention to the requirments of“ ... more

HomeIFA for Data RecipientsData provision

Data provision

”Within the parameters of data provision the data stock is delivered initially The subsequent updates can take place at individual fixed intervals The following data delivery modes are available for the provision of data and accompanying delivery information“ ... more

HomeIFA GmbHShareholders

Shareholders

”ABDA – Bundesvereinigung Deutscher Apothekerverbände e. V.Federal Union of German Associations of Pharmacists Heidestraße 7 10557 Berlin Bundesverband der Pharmazeutischen Industrie e. V. (BPI)German Association of Pharmaceutical Industry“ ... more

HomeFAQ

FAQ

”Under what circumstances is an article no longer subject to verification? | If a product is no longer subject to prescription, the verification obligation is usually also not required. The manufacturer is obliged to recall the product with the affected safety features and“ ... more

HomeIFA for SuppliersNotification order documents

Notification order documents

”You may submit your notification orders to IFA GmbH using excel order files XLSX format Please fill in a complete order and send it by email to ifa@ifaffm de Further information on how and when notifying an order as well as explanations to each order type and“ ... more

HomeFAQ

FAQ

”Where can I find the legal background on verification? | Legal background to verificationcan can be found here: Falsified Medicines Directive 2011/62/EU (FMD) Delegated Regulation (EU) 2016/161 (dVO) Further information can be found here: FAQ of the EU“ ... more

HomeFAQ

FAQ

”I want so sell my product through pharmacies. Under which conditions can I receive a Pharmazentralnummer (PZN)? | Receiving PZN and their publication requires the signing of IFA's supplier contract outlining the buisiness relations.A PZN is issued while product data are“ ... more

HomeFAQ

FAQ

”May I hand in 'Zulassungs- / Registrierungsunterlagen' late? | The regular deadline applies to the publication of medicinal products obliged to marketing authorisation or mandatory registration into IFA's Database. IFA's Publication Calendar states all deadlines for their“ ... more