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Expert support

A reliable expert at your side

We understand the complexities of regulatory pathways and the critical importance of scientific integrity in this field. After two decades of experience, we are proud to be the trusted partner of over 180 industry leaders and innovators. 

Medical devices

Our expert team has extensive experience in handling all device classes, drug-device combination products, and in vitro diagnostic devices.

Pharmaceuticals

IASON consulting can assist in a variety of drug-related needs from toxicology services to eCTD compilation in all molecule classes.

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Fresh ideas

Due to our helicopter perspective and experience, we can bring fresh ideas and innovative approaches that have proven successful before. 

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Instant clarification

Instant access to solutions for regulatory, scientific, strategic, or process-related issues significantly accelerates the completion rate of projects.

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Objective perspective

As external consultants, we offer an objective perspective that can be crucial in spotting issues and opportunities that internal staff, often too close to the project or organization, might miss.

Expert support

Where our experts excel

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Regulatory strategy & compliance

Guidance on meeting regulatory requirements and strategies for successful submissions to regulatory bodies.

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Product safety & toxicology

Evaluating and mitigating risks associated with the use of products to ensure patient safety and product efficacy.

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Study design & support

Expertise in planning and executing clinical trials, biocompatibility evaluation & testing, ensuring scientifically sound and compliant study designs.

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Product development

Allowing a clear regulatory pathway concept beginning at the conceptualization stage for the smoothest possible submission. 

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Expert support

Digital health

With the growing importance of software in or as medical devices, including AI and machine learning, our consultants provide guidance on software development including DiGA (digitale Gesundheitsanwendungen), validation, and compliance with relevant standards and regulations.

Access to industry veterans

Access to industry veterans can profoundly impact health projects by bringing in a wealth of experience and deep insights.

They can assist in comprehending strategic or regulatory requirements and provide ingenious solutions drawn from their many years of expertise.

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Frequently asked questions

Didn't find the answer you were looking for? Connect with us using our Contact form

  • Molecule classes
    We can support you with our expertise across the full spectrum of drug development: from small to large molecules, biologics to oligonucleotides and more.
  • Development stages
    TODO
  • Species selection
    TODO
  • Technologies
    e.g. silencing novel approaches?
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