EUROPE

Clinical Research Operations and Study Support

Across Europe

CEBIS’s established European presence supports international clinical research delivery through operational teams and study logistics coordinated with the organization’s wider clinical, regulatory, data and safety capabilities.

EUROPEAN PRESENCE

Current CEBIS Locations

in Europe

CEBIS has operational locations in Switzerland and Romania and a logistics location in Ireland.

SWITZERLAND · HEADQUARTERS

Lugano

Lugano Business Centre
Via Maggio 1C
6900 Lugano
Switzerland

Phone: +41 91 260 15 75
Mobile: +41 44 585 20 24

ROMANIA · ADMIN HUB

Bucharest

Helios Business Center
47 Theodor Pallady Avenue
Entrance B, 3rd Floor
Bucharest 032258
Romania

Phone: +40 21 320 32 81
Mobile: +4 (0) 721 839 837

IRELAND · LOGISTICS

Dublin

11-15 Tara Street
Dublin 2, D02 RY83
Ireland

CLINICAL DELIVERY

Study Coordination Across

European Markets

European studies can involve several countries, authorities, ethics bodies, investigative sites and supporting vendors. CEBIS connects the required activities through a coordinated study model.

Study Planning

Align participating countries and operational requirements with the protocol.

Site Management

Coordinate sites through feasibility, start-up, monitoring and closeout.

Project Management

Maintain milestones, responsibilities and cross-country communication.

Data & Statistics

Use consistent study-data and statistical processes across participating locations.

Safety

Coordinate pharmacovigilance and medical-monitoring activities.

Regulatory Affairs

Support European regulatory planning, Clinical Trial Applications, ethics coordination and amendments.

LOGISTICS

Supporting Clinical Material Movement Across Study Sites

CEBIS’s Dublin location supports study logistics that may include site shipments, clinical materials, consumables, shipment tracking, cold-chain requirements, equipment logistics and country-specific import requirements.

MULTINATIONAL DELIVERY

Keeping Multiple Countries Within One Study Plan

International trials work best when country-specific activities remain connected to central study leadership.

European Sites
Country Requirements → Project Management → Data & Safety → Supply & Logistics → Sponsor Communication

European activities can also be coordinated with CEBIS locations in the United States, Canada and India when appropriate to the study.

Planning a European Clinical Program?

Tell us about your product, development stage, target countries, study design, sites and required services.