Service Portfolio
Our main objective is to make things happen through committed and professional execution. We provide a full range of services, including:
Clinical Research Management - Clinical Phase I-IV & NIS/PMS/PASS*:
- Study Concept & Study Development: commercial & non-commercial studies (IIT*)
- Study Steering Committee / Advisory Board setup and management
- Study Implementation, Supervision & Coordination
- Trial Management & Site Monitoring & Site Management
- CRO Management
- eCRF Development
- Regulatory Affairs (IRB/IEC/HA submission)
- Data Management & Safety Surveillance
- Clinical Quality Assurance - Auditing & Audit preparation
- Medical Writing & Translation Services
- Training Services for Investigators, CROs, Site Management
Medical Marketing & Strategic Consultancy Services:
- Clinical Development Strategy
- Medical Marketing
- Study Marketing
- KOL-Program Development and Implementation
- Expert / Advisory Network Development, Publication Boards, etc.
- Scientific Meeting Organization: Investigator Meetings / Symposia / Congresses
- Patient Advocacy Group interactivities
- Scientific Communication and Medical Writing
- Training (Product specific, Field Force, CRO, Compliance, etc.)
- Sales Management Support
Our services comply with all applicable legal, regulatory and ICH-GCP regulations and guidelines as well as our customers' SOPs.
* NIS – non-interventional studies; PMS – post-marketing surveillance studies; PASS – post-authorization surveillance studies; IIT - Investigator initiated trials