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What we do
Seven services, one coordinated partner — from first-in-human through patient access.
01
Clinical development is more than trial execution — it is a strategic journey that transforms innovation into evidence, from first-in-human studies to post-marketing research.
02
We bring clinical research closer to patients through flexible, decentralised and hybrid trial approaches — digital practice with experienced clinical oversight.
03
Running a medical device or diagnostics trial is not a copy of a pharmaceutical model. CORONIS builds strategies that fit the science, speed, and compliance landscape of medtech.
04
Regulatory support across study start-up, clinical trial submissions, product registration, market access, and post-authorisation activities — European and national.
05
End-to-end pharmacovigilance aligned with GVP and European/local legislation, complemented by medical device vigilance and cosmetovigilance.
06
Quality compliance and auditing to identify gaps, prevent deviations, and keep programs inspection-ready.
07
Adherence programs that combine personalised care with practical support — education, delivery, counselling, and 24/7 safety — so treatment becomes a path to wellbeing.
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Whether you need a full-service CRO, a local partner in Greece and Cyprus, or a patient support program, we will map the work with you.