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Innehållstyper
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100 000 timmar av beprövad tillförlitlighet: KNF:s membranpumpar sätter en ny standard
Tillförlitlighet är inbyggd i varje KNF-pump. I ett långtidstest uppnådde KNF:s membranpump NMP 850.1.2 mer än 100 000 driftstimmar under definierade testförhål...
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Strengthen your team with Clinical and Regulatory Experts
Not every challenge calls for a permanent hire.
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Clinical and regulatory expertise that delivers results
Organizations in the life sciences sector are under constant pressure to meet regulatory requirements, maintain clinical study timelines, and ensure inspection ...
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Medtech Compliance Forum by Aurevia & RAPS
We are excited to announce that registration is now open for the Medtech Compliance Forum by Aurevia & RAPS, taking place as part of Labquality Days 2027 in Helsinki, Finland.
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Experienced clinical and regulatory support for a busy autumn
The post-summer backlog is real.
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Expanding into the EU market?
Expanding into the EU market as a medical device or IVD manufacturer? For non-EU/EEA companies, appointing a European Authorised Representative (EAR) is not jus...
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Att välja rätt material för membranpumpen
Att välja rätt material för membranpumpar är avgörande för att säkerställa tillförlitlig, säker och kontamineringsfri drift i industriella tillämpningar. Materi...
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Flexible clinical research support for your urgent project needs
When resources are stretched or timelines are tight, waiting is not an option.
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Streamline medical device development with an integrated platform
Developing medical devices (MD) today means navigating complexity—regulatory requirements, documentation, risk management, and fast-moving innovation. What if y...
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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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Strömberg Distribution – logistik, beredskapslager inomLife Science
Strömbergs centrala del av verksamheten är inom Life Science och möjligheten till beredskapslager, där kritiska produkter lagras för att garantera leveransförmå...
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Keep projects on track this autumn with Senior Clinical and Regulatory Expertise
Where could senior clinical and regulatory expertise make the biggest impact this autumn?
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UK Responsible Person: A critical partner for UK market access
If you're a non-UK manufacturer, appointing a UK Responsible Person (UKRP) is mandatory for placing medical devices and IVDs on the UK market.
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First Patient Enrolled in International Phase III Clinical Trial
We are proud to announce that the first patient has been enrolled in an international Phase III clinical trial investigating a treatment for bacterial vaginosis.
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Customer success stories: Advancing quality, regulatory and clinical research excellence
Strong partnerships drive successful outcomes.
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5 reasons to choose Aurevia as your quality, regulatory and clinical research partner
In today’s complex life sciences landscape, success depends on working with a partner who understands both the regulatory environment and the realities of clinical research.
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Medtech Compliance Forum by Aurevia & RAPS - part of Labquality Days
Aurevia is pleased to announce a new partnership with RAPS, the Regulatory Affairs Professionals Society, to strengthen the medtech programme at Labquality Days...
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En tyst besparing - Hur vakuumpumpar minskar energiförbrukningen i labbet.
Varje watt räknas i moderna laboratorier. Upptäck hur byte till torrgående scrollvakuumpumpar kan sänka både elkostnaderna och kylningsbehoven, förbättra hållba...
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Tailored eQMS solutions - book a free demo
Struggling to manage quality processes efficiently as your organization grows?
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EDIH Summit 2026 Finalist: Simplifying Regulatory Compliance
Excited to be recognized as one of five European Digital Innovation Hub (EDIH) Community Award finalists at the EDIH Summit 2026!
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How Forsante uses AI and automation for better quality of care
Forsante Oy’s MDR-certified IRMA decision engine helps automate clinical processes, reduce manual work, and supports more consistent treatment pathways.
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Most people underestimate what data management really means in medtech and IVD
In pharma, data management is typically focused on getting clean, consistent, and traceable clinical data—which means that data anomalies are usually handled du...
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Aurevia expert spotlight: 3 questions with our risk management expert
Meet Cristina Albu Barkman, Principal Consultant, and one of Aurevia’s most experienced specialists in medical device risk management. With more than 25 years i...
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Aurevia - your partner for oncology clinical trials
Oncology trials are complex—scientifically, operationally, and from a regulatory perspective. Our teams have both deep knowledge and hands-on experience, suppor...
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