Who we are

PharmaLex Denmark A/S, previously known as Jacobsen Pharma A/S and Lindeq A/S, has been a service provider within Regulatory Affairs, Pharmacovigilance, Medical Writing and Quality Assurance since 1995. In July 2016 we became part of the PharmaLex Group. With more than 1000 colleagues around the world we can be your local partner with a global reach.

We are more than 15 highly specialized and competent consultants in the Danish office – which is located in Hørsholm near Copenhagen. We can support you either on site (at your facilities) or you could outsource all or parts of your activities to the team in our Danish office.

  • Like all PharmaLex affiliates, PharmaLex Denmark is capable of offering the entire service portfolio the group has to offer, making sure our clients receive the same high standards they have to come to expect.
  • PharmaLex Denmark offer international support for client products with excellent expertise locally supported by subject-specific experts, a great pool of experience as well as a swift deployment of regional and highly qualified staff covering your short-term demand.

Local Contact

  • Torben Nørgaard
    General Manager PharmaLex Denmark Agern Allé 24
    DK-2970 Hørsholm
    Denmark
    +45 78 79 95 05

What our clients say about us

We are working with a number of large pharma companies and are looking to create a consortium of partners to collect feedback on expertise, availability and outcomes. If you would be interested in joining our consortium, please contact us on contact@pharmalex.com.

  • Pharmalex provided the resources we needed to compile Investigational Medicinal Product Dossiers for our biological products. The dossiers were delivered on time with the trusted quality we expected

    Small US Biopharmaceutical Company
    Sr Director Regulatory Affairs CMC
  • We needed a partner to help us obtain device approval. PharmaLex have not only helped us achieve this but are now providing on-going post-marketing surveillance support. We would highly recommend them to anyone who needs specialist expertise.

    Med Device company, US
    Senior Regulatory Affairs Director
  • Able to explain technical details so non-experts can understand

    US based small / virtual company
    Partner
  • There was a close relationship between the regulatory strategy and the writing activities. You developed a fine-tuned regulatory strategy which will be a key factor to smooth the approval of our dossier.

    Large Pharma, Global
    VP Regulatory Strategy