International Marketing

  • Post-marketing surveillance
  • Marketing concepts, product profiles
  • Development of promotion concepts
  • P R for professionals and general public
  • Organisation of continuing educational events and conventions
  • O T C management
  • Sales structures for domestic and international production
  • Projects for reimbursement and economic issues
  • Patient education, consumer response (for example compliance)
  • Disease management
  • License brokering
  • Employee product training
  • Regulatory affairs

Service Overview
- Clinical Research
- International Marketing
- Standards
Our

EMEA Pharmacovigilance · Health care studies · Observational studies · EMA Pharmacovigilance · Medical Biometrics · Approval of Medical Devices · Pharmacovigilance · Clinical Investigators · Clinical Trials · GCP Legislation · GCP - Good Clinical Practice · ICH GCP E6 · GCP Guidelines · GCP Compliance · BfArM GCP · CRO – Clinical Research Organisation · CRO – Contract Research Organisation · PSUR · PSURs · Pharmacoeconomics, Health · Pharmacoeconomic studies · Pharmacoeconomics · Patient Monitoring · Monitoring Clinical Trials · Clinical Monitor · Marketing Authorisation · Medicinal Product Approval · Drug safety · Data management plan · Clinical development · Monitoring investigators · Non-interventional studies (NIS) · Patient recruitment · Phase IV studies · Investigator audit · Investigator qualification · Investigator selection