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ePI isn’t just an IT project. It touches regulatory, translation and your whole labelling process. So why juggle several providers? We cover the full journey for you, from the first assessment and regulatory questions through to FHIR conversion, validation and all EU languages. We’ve been working on product information since 1998. Let’s talk at TOPRA in Utrecht, booth 11, 19 to 21 October. #ePI #RegulatoryAffairs #TOPRA

Is your product information ready for HL7 FHIR? We take your SmPCs, package leaflets and labelling from Word or PDF and turn them into validated ePI that meets the EU ePI Common Standard. Translated into every EU language, of course. Come and see us at TOPRA in Utrecht. You’ll find us at booth 11 from 19 to 21 October. #ePI #RegulatoryAffairs #TOPRA

Jessica, Anastasia and Samuel are heading to TOPRA in Utrecht next week. If you’re wondering how to get your product information from Word or PDF to validated, translated ePI, they’re the people to talk to. Drop by booth 11 between 19 and 21 October. Or send us a message beforehand and we’ll set up a time that suits you. #ePI #RegulatoryAffairs #TOPRA

With the new EU Pharma Legislation, the shift towards electronic product information is accelerating. mt-g ensures your data is compliant, structured, and ready for submission.

Our ePI solutions combine regulatory knowledge with multilingual translation to make your product information accessible across markets.

In the field of medicinal product authorizations, ePI is currently on everyone's lips - thanks to the transformation of documents into the XML FHIR format, files can be imported directly into the PLM portal, making the authorization process more efficient. At mt-g, we can support you even better in your authorization process with our file transformation solution.