Laboratorio de Biofarmacia y Farmacocinética (LABIOFAR)

The Laboratorio de Biofarmacia y Farmacocinética (LABIOFAR) was created in 1985 to respond to the needs of the country regarding the new regulations for the registration of pharmaceutical products.
Its activity includes biopharmaceutical analysis and pharmacokinetic studies through basic and applied research projects or through research contracted by pharmaceutical companies both nationally and internationally. It also develops training for professionals from the pharmaceutical industry, health authority, academia and social security at the national level as a Central American.


LABIOFAR has supported the Directorate of Records and Controls of the Ministry of Health in the elaboration of bioequivalence regulations for the registration or renewal of sanitary registration of medicines that require it.


It is the only laboratory of its kind in Central America and the studies provides valuable information on the quality of the medicines investigated to guarantee the interchangeability of generic drugs with the corresponding original products.

 

Services

Its activity includes biopharmaceutical analysis and pharmacokinetic studies through research projects  by pharmaceutical companies both nationally and internationally. Learn more about our analytical services in this link.

It also develops training for professionals from the pharmaceutical industry, health authority, academia and social security at the national level as a Central American. Please visit this link  for more information about our training.

 

Contact info

Coordinator: Dr. Nils Ramírez

Phone: 2511 8318
Lab telephone: 2511 8337
E-mail: inifar@ucr.ac.cr
Fax: 2511 3426

Projects

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Vigencia: 01/06/2014 al 31/12/2018

Descripción: El poyecto busca continuar con el estudio de diferents fases del estado sólido en materia prima farmaceútica y ampliarlo a formas de dosificación terminadas para detectar dentro de ellas cambio polimórficos o afines.

Vigencia: 01/01/2012

Descripción: El objetivo de este proyecto es establecer la metodología adecuada para cuantificar en fluidos biológicos principios activos de formulaciones multiorigen para la aplicación en futuros estudios de bioequivalencia.


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