Pre-clinical services

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Medical writing services for Life Science team

WE ARE NOT JUST A PROVIDER, WE WILL BE YOUR NORDIC PARTNER

SCIENTIFIC AFFAIRS SUPPORT THROUGHOUT THE WHOLE CLINICAL DEVELOPMENT

We outsource specialists and offer ad-hoc support to our clients. We will help you to get new pharmaceuticals, products, methods, and devices to the market faster!

We develop your organization with our highly competent consultants. Our experts add more than just skills and competence, they add experience and know-how from the industry and many different companies. We work across all Nordic countries.

Our main goal is to work closely together with you and solve your challenges in a flexible manner.

We offer you flexible solutions and take on both smaller projects involving only one expert and a few hours as well as and bigger projects involving several competences. We solve peak capacity challenges and help you with limited projects.

Clinical studies consultant team of three

PRE-CLINICAL SERVICES

  • Strategies moving from pre-clinical to clinical phase
  • IND-enabling pre-clinical program
  • Gap analysis
  • Define starting dose for first-in-man clinial trial
  • Pre-clinical study design
  • CRO selection and oversight
  • Study report writing and review

Contact:
Margrethe Erbou Andersen
Nordic Head of Regulatory Affairs
+45 3590 1129 | margrethe.andersen@pharmarelations.dk

Emma P_Webben

Emma Perlhamre

Nordic Head of Clinical Development

If you have any questions, please feel free to contact Emma directly
– she will be happy to help you.

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