Cyprus · Clinical Bridge · Radiopharmaceuticals

Where radiation
meets transformation.

Daughter of Helios. Pharmakeia.

Cyrcea connects novel radiopharmaceutical developers with nuclear medicine departments in Cyprus for early-phase clinical evaluation — bridging R&D innovation with first-in-human studies within the EU.

Named for Circe, daughter of Helios — goddess of transformation and the original Greek pharmakeia. The ancient word for those who make medicines.

What we do

The bridge between
discovery and clinic.

We act as the structured pathway between radiopharmaceutical innovators and accredited nuclear medicine departments — enabling Phase I studies in an EU-regulated, cost-efficient, and scientifically rigorous environment.

For R&D Developers

We provide a fully managed pathway to evaluate your novel diagnostic or therapeutic radiopharmaceuticals in Phase I clinical studies — from regulatory strategy to patient access.

For Nuclear Medicine Departments

We bring cutting-edge compounds to your department, handling the commercial, contractual, and coordination layer — so your clinical team can focus on science and patient care.

Diagnostic Radiopharmaceuticals

Novel PET and SPECT tracers for oncology, neurology, and cardiology — evaluated through structured imaging studies with rigorous biodistribution and dosimetry protocols.

Therapeutic Radiopharmaceuticals

Targeted radionuclide therapy compounds — including alpha and beta emitters — evaluated under GCP-compliant Phase I frameworks with full dosimetry and safety monitoring.

The model

A single point of
connection. End to end.

Origin
R&D Developer
Novel compound. Preclinical data. Ready for first-in-human evaluation.
Bridge
Cyrcea
Regulatory strategy, site liaison, protocol design, ethics, coordination, data management.
Destination
Nuclear Medicine
Accredited Cyprus nuclear medicine departments. Phase I execution. EU-regulated.
Outcome
Phase I Data
Safety, PK, dosimetry, and imaging data. First-in-human evidence package.
EU jurisdiction EMA regulatory framework GCP compliant Phase I Theranostics PET / SPECT Alpha & Beta emitters
EU Regulatory jurisdiction
Phase I Clinical focus
Both Diagnostic & therapeutic
Island Cyprus, Mediterranean

Why Cyprus

Strategic, regulated,
and agile.

01
EU member state

Full EMA regulatory framework. Data generated in Cyprus is valid across all EU member states and accepted in international regulatory submissions.

02
Cost efficiency

Substantially lower Phase I operational costs compared to Western European hubs, without compromising scientific rigour or GCP compliance standards.

03
Speed to ethics

Agile national ethics and competent authority review timelines. A focused, smaller regulatory environment enables faster study initiation.

04
Nuclear medicine infrastructure

Accredited nuclear medicine departments with established PET, SPECT, and dosimetry capabilities ready for early-phase evaluation.

05
Strategic location

Gateway between Europe, the Middle East, and North Africa. Ideal for sponsors seeking EU registration while maintaining proximity to emerging markets.

06
English-language environment

Medical, regulatory, and legal infrastructure operates fully in English — minimising friction for international sponsors and reducing documentation overhead.

Get in touch

Begin the conversation.

Whether you are an R&D developer with a compound ready for evaluation, or a nuclear medicine department interested in partnership — we would like to hear from you.

Headquarters
Nicosia, Cyprus
European Union
General enquiries
info@cyrcea.com
Regulatory & clinical
clinical@cyrcea.com
Business development
partnerships@cyrcea.com

"Κίρκη — she who transforms. Daughter of the sun. Maker of medicines. From her island, she changed the nature of things."

— Homer, The Odyssey · Our namesake