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Regions

spainbelgium-netherlandsgermanypolandrussiaukrainehungarycroatiaromaniamoldovaserbiabulgaria

Germany
CCDRD AG Headquarter Hoppegarten, near Berlin

  • General Management
  • Business Development
  • Regulatory and Strategic Advice
  • Clinical Operations
  • Project Management of phase I-IV trials
  • Submission services
  • Monitoring of phase II-IV trials in Germany
  • Statistics and Data Management
  • Quality Managment
  • Information Technology
  • General Services / Administration

Bulgaria
Sofia

  • Management of three local Phase I units
  • Site identification and management for phase I-IV trials
  • Feasibility evaluation
  • Strong clinical networks and access to qualified sites in oncology, CNS, renal disease, diabetes, dermatology, diabetes, cardiology
  • Regulatory submissions
  • Specialized monitoring of pharmacokinetic studies
  • Monitoring of phase I-IV studies

Poland
Poznan

  • Feasibility evaluation of clinical sites
  • Site identification and contracting
  • Strong clinical networks and access to sites in oncology, renal disease, metabolic disease, diabetes, dermatology, ophthalmology
  • Regulatory submissions
  • Monitoring of phase II/III studies

Serbia
Belgrade

  • Feasibility evaluation of clinical sites
  • Site identification and contracting
  • Regulatory submissions
  • Monitoring of phase II-III studies

Croatia
Zagreb

  • Feasibility evaluation of clinical sites
  • Site identification and contracting
  • Strong clinical networks and access to sites in oncology, renal disease, metabolic disease, diabetes, dermatology, ophthalmology
  • Regulatory submissions
  • Monitoring of phase II/III studies

Russia
Moscow, St. Petersburg

  • Feasibility evaluation of clinical sites
  • Site identification and contracting
  • Strong clinical networks and access to sites in oncology, renal disease, metabolic disease, diabetes, dermatology, ophthalmology
  • Regulatory submissions
  • Monitoring of phase II/III studies

Ukraine
Kiev

  • Feasibility evaluation of clinical sites
  • Site identification and contracting
  • Strong clinical networks and access to sites in oncology, renal disease, metabolic disease, diabetes, dermatology, ophthalmology
  • Regulatory submissions
  • Monitoring of phase II/III studies

Hungary
Balatonalmádi

  • Feasibility evaluation of clinical sites
  • Site identification and contracting
  • Strong clinical networks and access to sites in oncology, renal disease, metabolic disease, diabetes, dermatology, ophthalmology
  • Regulatory submissions
  • Monitoring of phase II/III studies

Moldova
Chisinau

  • Feasibility evaluation of clinical sites
  • Site identification and contracting
  • Strong clinical networks and access to sites in oncology, renal disease, metabolic disease, diabetes, dermatology, ophthalmology
  • Regulatory submissions
  • Monitoring of phase II/III studies

Romania
Timisoara

  • Feasibility evaluation of clinical sites
  • Site identification and contracting
  • Strong clinical networks and access to sites in oncology, renal disease, CNS, diabetes, dermatology
  • Regulatory submissions
  • Monitoring of phase II/III studies

Spain
Barcelona, Madrid, Valencia

  • Feasibility evaluation of clinical sites
  • Site identification and contracting
  • Strong clinical networks and access to sites in oncology, renal disease, metabolic disease, diabetes, dermatology, ophthalmology
  • Regulatory submissions
  • Monitoring of phase II/III studies

The Netherlands and Belgium

  • Feasibility evaluation of clinical sites
  • Site identification and contracting
  • Strong clinical networks and access to sites in oncology, renal disease, metabolic disease, diabetes, dermatology, ophthalmology
  • Regulatory submissions
  • Monitoring of phase II/III studies
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