Investigación bioanalítica-estudios de bioequivalencia

May 10, 2018 By rperez

Sistemas de robótica [/Caption] laboratorios ADPEN proporciona pruebas para estudios de bioequivalencia. Contamos con el equipo para realizar bioanálisis de muestras derivadas de fases clínicas de estudios de bioequivalencia en nuestras instalaciones de vanguardia. ADPEN tiene la ventaja competitiva mediante la utilización de sistemas automatizados que proporcionan rentabilidad y atrae proyectos de investigación de contratos internacionales (bioequivalencia) que actualmente hacen su camino hacia los Cro fuera de los Estados Unidos.

ISO/IEC 17025 is a company level accreditation based on a standard published by the International Organization for Standardization (ISO) titled “General requirements for the competence of testing and calibration laboratories”. ISO/IEC 17025 is a general umbrella term used to refer to the specific standard; the current version of this standard is ISO/IEC 17025:2017. The standard contains two main sections: management requirements (primarily related to the operation and effectiveness of the quality management system within the laboratory) and technical requirements (primarily related to the competence of staff and calibration of equipment). The standard also gives requirements related to quality management such as document control and corrective action. This standard is the basis for accreditation from an accrediting body.

ADPEN has also been inspected by the US-EPA and US-FDA multiple times with no observations.

Investigación bioanalítica-estudios de bioequivalencia

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