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CYTUVA

Center for studies on the safety of medicines (CESME)

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Contact Information

Basic Information

  • UniversityUniversidad de Valladolid
  • Center
  • Department-
  • Investigation GroupCenter for studies on the safety of medicines (CESME)


Description

The center for studies on the safety of medicines (cesme) is an interdisciplinary center of the University of Valladolid dedicated to research on the safety and effects of medicines on human populations. The cesme has its origin in the experience and work developed in the field of drug safety, since 1986, by the team of professors, researchers and technicians of the Center for Pharmacovigilance of Castilla y León. The creation of cesme as a University Center was approved in 2010 by the University of Valladolid; it had previously been constituted as a University Institute (Institute of Pharmacoepidemiology - IFE). This condition allows the cesme to contract with public or private entities to carry out scientific or technical work and studies, as well as to teach specialization courses. The cesme is part of the Recognized Research Group (GIR) of Pharmacogenetics, Cancer Genetics, Genetic Polymorphisms and Pharmacoepidemiology of the University of Valladolid. The ultimate goal of the Center is to help improve the health of individuals through the most appropriate use of medications.

Pharmacoepidemiology, the field of knowledge in which the Center's work is framed, addresses the study of the effects of drugs on human populations. It uses the epidemiological method and is a meeting point between clinical pharmacology and epidemiology. It is, therefore, a matter of applying epidemiological knowledge, method and reasoning to the study of both the beneficial and adverse effects of drugs; interpreting the effects of drugs also requires a sound understanding of pharmacology. In addition, pharmacoepidemiology has the task of knowing the way in which drugs are used. 

UNITS:
  • PharmacoVigilance Center: The Center for Drug Safety Studies began pharmacovigilance tasks in Castilla y León in 1986 as a pilot center. In 1987 it received accreditation as a Pharmacovigilance Center by the National Pharmacovigilance Commission and today it continues to carry out this activity. The Castilla y León Pharmacovigilance Center is part of the Spanish Pharmacovigilance System for Medicines for Human Use (SEFV-H).
  • Pharmacogenetics Unit:
    • Genome Whole Association Studies (GWAS)
    • Studies of genetic polymorphisms associated with drug-induced adverse reactions
    • Search for candidate genes and location of SNPs.
  • Meta-analysis Unit: All our systematic reviews / meta-analyzes are registered in the Prospective International Registry of Systematic Reviews PROSPERO as a guarantee of their suitability and prospectivity (Shamseer L et al. BMJ 2014; 349: g7647)


Other information

Number of researchers:

15

Technological Line(s):

- Laboratories and research centers

Development status:

In research and development phase

Differentiation in the market:

Quality

Applicability of technology:

Yes

Additional Information:

ENCePP statement
We are a center associated with the ENCePP scientific network, coordinated by the European Medicines Agency. We are dedicated to excellence research following the ENCePP Guide on Methodological Models and promoting scientific independence and transparency. We use the ENCePP Electronic Study Register, a publicly accessible tool for registering pharmacoepidemiology and pharmacovigilance studies.

UNESCO Code:

3299 - Other medical specialities

Other members:

Eutiquia León Rodríguez
María Sáinz Gil
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Virginia Delgado Armas
Natalia Jimeno Bulnes
Verónica Velasco González
Carlos Treceño
Pilar García Ortega
Rosario Sanz Fadrique
María Isabel Jiménez Serranía

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Related projects

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