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.

  • Provided honest feedback and collaborative working solutions to obstacles

    South Korea based medium sized company
    Manager
  • Thanks so much for your support over the past 30 days. Your commitment and timely communication have made working with you all a pleasant experience.

    US Biotech
    Senior QA Associate
  • I just wanted to relay our sincere thanks to you and the team for two really excellent days training. It was well organized and structured to cover regulatory expectations, GMP principle and routine work challenges of industry. The presenters and moderator were highly skilled in this area to accommodate any queries raised during the training session and were well able to keep the team engaged even in remote/virtual training session. The design of training slides was impressive and the use of technology to make virtual training was remarkable.

    Lorraine Henry
    Compliance Lead, Qualified Person, Amneal Ireland Limited
  • We needed to develop our strategy and PharmaLex had exactly the experience we needed.

    Med Device company, UK
    Senior QA Director