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Klinische Forschung Gruppe Nord

Patients. Efficiency. Quality.

Klinische Forschung Gruppe Nord

Klinische Forschung Gruppe Nord - KFGN - is a network of seven independent clinical research sites in Germany. Our sites are located in Hamburg, Hannover, Schwerin, Kiel, Berlin, Dresden and Karlsruhe. We are specialized in conducting clinical trials under high quality standards and with effective recruitment opportunities.

Our staff is highly experienced and qualified - at each site you will find in-house investigators, study coordinators, study nurses and recruitment manager. We are able to offer the capabilities and the equipment to conduct clinical trials in various indications. For example internal medicine, cardiology, pneumology, neurology, dermatology, paediatrics, oncology, ophthalmology and more. We are a reliable partner ensuring high quality data and the safety of our patients.

Our sites are centrally managed in the fields of feasibility management, qualitiy management, marketing, contract management and accounting. This means a great advantage to our partners - few interfaces, efficient and fast communication, central contact persons additional to the close contact to the study teams at the sites.

Web Site: www.kfgn.de 

Information

Demographic Data

  • SITE INFORMATION 
  • Start year clinical research1995
  • Phases of clinical studiesPhase I, Phase II, Phase III, Phase IV
  • Types of studiesBiologics, Drugs, Medical Devices, Nutraceuticals, Vaccines
  • PopulationsInfant 0-1yr, Child 2-10 yrs, Adolescent 11-17 yrs, Adult 18-64 yrs, Senior 65 yrs and over
  • SPECIFIC SITE INFORMATION 
  • Type of siteFreestanding
  • # of employees involved in researchoverall up to 100 employees at our 7 sites
  • # of investigatorsoverall about 30 investigators at our 7 sites
  • Number of studies last year20
  • Days openMonday, Tuesday, Wednesday, Thursday, Friday
  • Extended office hoursYes
  • Overnight facilitiesYes
  • Dry iceYes
  • Blinded pharmacistYes
  • Dedicated monitoring spaceYes
  • Internet access for the monitorYes
  • Onsite laboratoryYes
  • Central laboratoryYes
  • Infusion capabilityYes
  • Shipping optionsFedEx, UPS, DHL, Other
  • REGULATORY INFORMATION 
  • Contact for regulatory documentsstudy coordinator at the corresponding site
  • Regulatory phone numbervia study coordinator at the corresponding site
  • # of days to turn around regulatory documents5-7 working days
  • Type of IRB used by this siteLocal
  • How often does your local IRB meet?As needed
  • Appropriate storage facilities for productYes
  • Able to appropriately store Schedule II drugsYes
  • FINANCIAL INFORMATION 
  • # days to turn around budget and contract10-14 working days