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News archive

  • Introducing NNIT Singapore

    Following the acquisition of HGP in April 2019 and due legal processes, HGP’s Asia branch recently became NNIT Singapore Pte Ltd.

  • Lægemidler skal være sikre

    Vi bad Jesper Borgstrøm, Advanced Advisory Consultant, i NNIT Life Sciences – Regulatory Affairs, om at guide os gennem de sikkerhedsprocedurer, der gælder for en af verdens mest regulerede produktudviklings og -produktionsprocesser.

  • New cool Cloud service from NNIT

    New cool Cloud service from NNIT A/S that will benefit all Life Sciences companies. Life Sciences is our DNA: http://bit.ly/2fF0qfR

  • Have you initiated the IDMP readiness phase?

    Pharmaceutical companies will soon be required to submit data in accordance to the ISO IDMP standard in the EU region.Have you initiated the #IDMP readiness phase? Be ready and read more here. 

  • NNIT and SAS Institute enters strategic collaboration on ISO IDMP

    Right now, Danish and European pharmaceutical companies are gearing up to comply with the ISO standards – designated IDMP – that come into force in the EU on 1 July 2016. The ISO IDMP standards require information from many areas of the pharmaceutical business, including regulatory affairs, research and development, manufacturing and distribution.

  • Are you ready for ISO IDMP?

    Following the implementation of XEVMPD, new legislation, based on five new ISO IDMP standards, is due to come into force in 2016. Rune Ringsholm Bergendorff, advanced business consultant at NNIT, explains how pharmaceutical companies will need to adapt business processes across the whole organisation.