Centro Ricerche Cliniche di Verona - Clinical Research Centre of Verona - Italy

www.crc.vr.it

The Centro Ricerche Cliniche di Verona (CRC) was founded in 2005 by the G.B. Rossi Hospital and now it is a state organization under Verona University and G.B. Rossi Hospital ownership. The CRC is located on the 8th floor of the Hospital G.B. Rossi. The CRC is an ideal partner for every aspect of drug development (i.e. development plans, drug dose selection, appropriate pharmacodynamic or effective endpoints, the recruitment of suitable populations, tools to monitor drug safety and tolerability). A full range of Phase I and II services can be provided (e.g. first time in human, drug-drug interaction, pharmacokinetics, food effects, bioequivalence, POC studies) by means of an in-house Clinical Pharmacology Unit, equipped to a high standard expertise and operating in close connection with specialists. The majority of staff have had more than 15 year experience managing trials with Heathy Volunteers Subjects and Patients. Since June 2006 we have been carrying out a total of 110 clinical trials in most therapeutic areas sponsored by outstanding pharmaceutical industries. Volunteer database consists of approximately 1200 active male and female healthy volunteers, with a good level of education, that enables a better comprehension of our documents and activities. Clinical trials with patients are carried out in collaboration with Teaching Hospital Units. The CRC is in full compliance with International Good Clinical Practice (GCP) standards and it has a UNI EN ISO 9001:2008 certification carried out by BSI S.r.l. . In October 2013, CRC received the first EUCROF Quality Certificate for Early Phase Units.

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The Centro Ricerche Cliniche di Verona (CRC) was founded in 2005 by the G.B. Rossi Hospital and now it is a state organization under Verona University and G.B. Rossi Hospital ownership. The CRC is located on the 8th floor of the Hospital G.B. Rossi. The CRC is an ideal partner for every aspect of drug development (i.e. development plans, drug dose selection, appropriate pharmacodynamic or effective endpoints, the recruitment of suitable populations, tools to monitor drug safety and tolerability). A full range of Phase I and II services can be provided (e.g. first time in human, drug-drug interaction, pharmacokinetics, food effects, bioequivalence, POC studies) by means of an in-house Clinical Pharmacology Unit, equipped to a high standard expertise and operating in close connection with specialists. The majority of staff have had more than 15 year experience managing trials with Heathy Volunteers Subjects and Patients. Since June 2006 we have been carrying out a total of 110 clinical trials in most therapeutic areas sponsored by outstanding pharmaceutical industries. Volunteer database consists of approximately 1200 active male and female healthy volunteers, with a good level of education, that enables a better comprehension of our documents and activities. Clinical trials with patients are carried out in collaboration with Teaching Hospital Units. The CRC is in full compliance with International Good Clinical Practice (GCP) standards and it has a UNI EN ISO 9001:2008 certification carried out by BSI S.r.l. . In October 2013, CRC received the first EUCROF Quality Certificate for Early Phase Units.

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Country

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City (Headquarters)

Verona

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Employees

11-50

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Founded

2005

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Potential Decision Makers

  • Clinical Trial Pharmacist

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    Phone (***) ****-****
  • Study Coordinator

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    Phone (***) ****-****
  • Consultant Dietitian

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    Phone (***) ****-****
  • Opera Viva! Summer Program for Singers and Teachers

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