Life Science og Health Care

Vores juridiske specialister har indgående og værdifuldt kendskab til Life Science industrierne og har derfor kommerciel forståelse for din virksomheds virkelighed.

Life Science og Healthcare jura er helt særegne discipliner, og området er kendetegnet ved konstant forandring­ og intensivering af både konkurrence og regulering.

Vi har fokus på hele processen fra ide og udvikling til det færdige produkt, og vores juridiske specialister tilbyder rådgivning inden for biotek, lægemidler, medicinsk udstyr, fødevarer og kosttilskud.

Vi bistår Life Science og Healthcare virksomheder med juridisk rådgivning, inden for følgende områder:

  • Kliniske forsøg
  • Immaterielle rettigheder
  • Patentretssager
  • Produktion og distribution
  • Salg og markedsføring
  • Transaktioner
  • Kontraktindgåelse
  • Produktudvikling
  • Retsforfølgelse
  • Konkurrenceret
  • Investering og udvikling

DELACOURs Life Science-specialister er faste undervisere i  brancheforeningerne Lægemiddelindustriforeningen (LIF) og Medicoindustrien. Derudover tilbyder vi intern undervisning og webinars til vores klienter om de særlige brancheregler. 

  • R&D

    R&D:
    We assist you in all legal matters related to the research & development of new treatments or devices. Be it protection of your intellectual property rights, clinical research agreements and transparency issues, GCP and the relationship with the health research ethics committee system.

  • Deals

    DEALS:
    An increasing number of co-operations within the life sciences industries require specialist advice from people who know the industry. Our dedicated team of life science specialists together with pragmatic and diligent specialists within mergers & acquisitions secure your deals. When you are co-developing, acquiring or selling IP-rights, forming joint ventures, investing or securing investments for future growth DELACOUR will help you strike the right deal.

  • Marketing authorisation

    MARKETING AUTHORISATION:
    When assisting life science companies with regulatory affairs, we draw on our deep experience in working with national and EU administrative authorities. We work in close co-operation with you and your specialists to make sure that your company navigates in the best possible way in the unique regulatory framework surrounding the life science industries.

  • Manufacturing

    MANUFACTURING:
    We understand the legal requirements for manufacturing a medicinal product, a device or a dietary supplement. We know it is like no other products, and we understand the efforts and investments required to secure safe, quality manufacturing.

  • Distribution

    DISTRIBUTION:
    Each country has its own unique systems of distribution of medicines and medical devices. We are highly specialized in this particular area of law. We know the challenges, we know the stake holders and the drivers within distribution, be it of OTC or prescription medicines, medical devices or dietary supplements.

  • Go to market

    GO TO MARKET:
    You are finally there. Ready to let your product reach the patients. You know how, and we know the unique law relating to advertising of medicinal products and medical devices, reimbursement, public tender processes and interaction with HCPs and patients.