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