Clinical research · Market access · Health technology
From clinical evidence to the clinic chair.
Medex generates the clinical evidence, opens the market and equips the clinic for medicines and medical devices – from Türkiye to Europe, the US and the Gulf.
A medical device manufacturer selling in Europe must collect real-world data on its product under the MDR.
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Medex brings the product to clinics in Türkiye. In AIDA, the clinic records the implant's reference and lot, follow-up visits and the patient's research consent; consented data leaves pseudonymised and encrypted.
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Medex CRO turns that data into the manufacturer's post-market clinical follow-up. One counterpart for market, evidence and follow-up.
Where we are
Operations in Türkiye; registered companies in five countries.