We transform Life Science

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Kim Raabymagle PharmaRelations
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Clinical experts in sponsor oversight
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Piia Rantala Recruitment
Headshot of Emma Perlhamre Sponsor oversight consultant

We create agility

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Courage-PharmaRelations values
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Senior recruitment manager in Life Science
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Pharmacovigilance
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We add expertise

Fredrik Anjou and Emma Perlhamre PharmaRelations
Clinical experts in sponsor oversight
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Headshot of Kim Raabymagle in Denmark.
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Headshot of Kristina Edholm

We take over non-focus areas

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Emma Perlhamre in meeting with other scientific affairs consultants
Smiley Life Science consultant
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Danish and Norwegian PharmaRelations Country managers
Headshot of Emma Perlhamre Sponsor oversight consultant
Medical team at PharmaRelations

We create value

Consultancy and outsorcing in Life Science
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Beatrice Öström and Sponsor oversight expert
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Consultant explaining Sponsor oversight
Margrethe Erbou Andersen
We support Nordic Life Science through all phases of development

FULL SERVICE PARTNER

Over the past 30 years, we have developed expertise across a wide range of services to help simplify Life Science operations for our clients across the Nordics. With the best experts and consultants we provide both edge and scope in our offerings.

Our key areas of expertise include Quality & Regulatory Affairs, Pharmacovigilance, Clinical Trials and Early Phases, Market Access, Commercialization, and Medical Engineering.

We tailor our services to meet our clients´ unique needs, offering a variety of solutions to address their challenges. Our solutions include Consulting, Outsourcing, Interim Support and Recruitment.

We are passionate about building long-term partnerships with our clients to consistently create great solutions together. Repeat clients and recurring business has been the foundation of PharmaRelations´ growth.

3 young PharmaRelations regulatory consultants
Available Positions

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Upcoming learning activities

04 September 2025
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Free webinar | Join us for this insightful webinar as we explore the new data governance section in Good Clinical Practice (GCP) guidelines.

Navigating the New Data Governance Section of ICH E6(R3)

16 September 2025
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Free Event: Afterwork invitation - Join us for an informal afterwork session and let's discuss the latest updates that will shape the future of our work

Let’s Talk AI in the context of Medical Devices & IVDs!

16 September 2025
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Free webinar | Join us for this insightful webinar as we explore what is required from you as a clinical trial sponsor.

Navigating Drug Safety in Clinical Development

12 Gazelle Awards

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Great Place To Work

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