SAI Global México

Iso/iec 17025 - lead assessor

SAI Global México
En Orlando (Estados Unidos)

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Información importante

Tipología Capacitación laboral
Lugar Orlando (Estados Unidos)
  • Capacitación laboral
  • Orlando (Estados Unidos)
Descripción

Who Should Attend?

Individuals wishing to perform audits to ISO/IEC 17025

Laboratory managers and supervisors

Companies seeking ISO/IEC 17025 accreditation

Companies that recognize the value of operating effective laboratory management systems

Registrar/Accreditation body Auditors

Existing (ISO 9001 / ISO/TS 16949) auditors who are looking to expand their skills in the area of laboratory practices

Supplier quality auditors wishing to evaluate laboratory service suppliers, including calibration suppliers

Instalaciones (1) y fechas
Dónde se imparte y en qué fechas
Inicio Ubicación
Consultar
Orlando
Florida, Estados Unidos
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Inicio Consultar
Ubicación
Orlando
Florida, Estados Unidos
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Preguntas Frecuentes

· ¿A quién va dirigido?

Who Should Attend? Individuals wishing to perform audits to ISO/IEC 17025 Laboratory managers and supervisors Companies seeking ISO/IEC 17025 accreditation Companies that recognize the value of operating effective laboratory management systems Registrar/Accreditation body Auditors Existing (ISO 9001 / ISO/TS 16949) auditors who are looking to expand their skills in the area of laboratory practices Supplier quality auditors wishing to evaluate laboratory service suppliers, including calibration suppliers

Programa académico

Key Session Topics


  • Overview of ISO/IEC 17025 requirements

  • Understanding the difference between quality management system registration and accreditation

  • Coordinating a quality management system audit against ISO/IEC 17025

  • Constructing an audit program and the preparation of audit checklists

  • Learning effective auditing techniques

  • Preparing nonconformity statements

  • Evaluating the significance of audit findings

  • Methods for improving communication skills

  • How to report audit findings and conclusions

  • Developing and implementing corrective action programs

  • Evaluating corrective action and understanding customer notification requirements

  • How to effectively follow-up audit findings to recognize if the nonconforming situation has been effectively resolved


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