Planning and reporting according to IVDR 2017/746 from Class A to Class D.
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Efficient continuous process of post-market surveillance for IVDs and medical devices.
Discuss your regulatory (MDD / MDR), developmental or strategic questions with our experts.
Do we really need a study? If so, how should our study look like, what are the best endpoints and where should we conduct it?
Professional literature searches by expert medical writers on new technologies, indications, targets, and more.
Receive 2nd opinions from industry veterans and gain confidence on strategic and scientific decisions.
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Be it medical device or pharma - IASON ensures that your health care project becomes a success.
projects completed
years of experience
clients around the globe
Medical writing, toxicology services, strategic and ad-hoc consulting.
Medical writing, toxicology services, strategic and ad-hoc consulting for medical device development and post-market surveillance.
IASON consulting is an established consulting firm that assists clients in medical device and drug development.
Our focus lies on scientific and regulatory support by providing key documentation and assessments as well as sharing our experience in toxicology.
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