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Integrated Clinical and Regulatory Support for Oncology Trials
Aurevia is a European Contract Research Organization (CRO) and regulatory partner supporting biotech, pharmaceutical, and medtech companies in the development a...
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QAdvis & Scandinavian CRO are now Aurevia
Two years ago, we became part of something bigger. At first, the change was mostly visible on paper — a new owner and later a new name: Aurevia.
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Imaging Core Lab and Clinical Adjudication in Clinical Studies
At Aurevia, we offer centralized adjudication and core lab services where experienced clinical experts, in close collaboration with our project managers, ensure...
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Clinical trials: proposals, budgets, and the evolving CRO role
This podcast episode from Trustful Clinical Budgeting dives into what really makes proposals work in clinical trials and why clarity, early alignment, and reali...
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Precision, balance and clinical experience
Phase II is often the most crucial phase of clinical development. This is where the study design is validated in practice, effect must be demonstrated, and wher...
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Insurance in Life Science: From risk to resilience
Are you visiting The Future of Swedish & Danish Life Science event in Lund 23 April? Don't miss the Gallagher seminar on Risk and Insurance in the Life Sciences sector.
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Clinical Evaluation in MedTech – Expert Insights from Sandra Sernbo for Building Safe Medical Device
The article highlights the role of clinical evaluations at GBA Key2Compliance in ensuring that medical devices are safe, effective, and ready for real-world cli...
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Strategic Clarity: The New Currency in Life Science
In an industry shaped by rapid regulatory changes and global competition, leading life science companies are rethinking what it takes to succeed. Increasingly, ...
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Advanced workflow automation and scalable image analysis in spatial biology
ZEISS and Concept Life Sciences announce partnership.
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Safety Data That Makes a Difference – Insights from Safety Manager Ida Björklund
The article highlights safety manager Ida Björklund’s approach to clinical trial safety. She emphasizes that all safety data, no matter how small, must be caref...
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Simplifying IVDR Compliance: Insights from Senior Consultant Emily Malmberg
Navigating the complex demands of the IVDR requires both strategic planning and deep regulatory insight. At GBA Key2Compliance, Senior Consultant Emily Malmberg...
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Why Less is More in Clinical Data – Insights from Senior Clinical Data Manager Åsa Testad
With a background in informatics and programming, Åsa Testad leads clinical data management at GBA Key2Compliance. She ensures that data in clinical studies is ...
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Gallagher – din försäkringsrådgivare inom Life Science
Med över 25 års erfarenhet av att leverera försäkring- & riskhanteringstjänster till life science-sektorn är vi på Gallagher ledande på området i Sverige. Som e...
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Utilising Clinical Strategy with Expert CRO Guidance from Key2Compliance
With the complexity of medical device regulatory compliance today, having a well-thought-out clinical strategy can help make the process smoother. In a nutshell...
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Key2Compliance tar över anrik steriliserings-utbildning
Kursen Sterilization of Medical Devices har funnits i över 30 år, och har examinerat hundratals personer. Nu tar Key2Compliance över kursen, som är den enda i s...
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Nordic Regulatory experts: Improving biotech chances of Succ
Why is it that so many biotech companies fail? And what are the tools needed to change that fact?
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QAdvis & Scandinavian CRO are now Aurevia
Two years ago, we became part of something bigger.
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