The document discusses statistical process control and statistical thinking. It outlines key concepts of statistical thinking including process and variation thinking. It emphasizes the importance of understanding variation and using data to quantify variation and measure effects in order to improve processes. It also discusses how statistical thinking can be applied at different levels from executives to managers to workers.
The document discusses statistical process control and statistical thinking. It outlines key concepts of statistical thinking including process and variation thinking. It emphasizes the importance of understanding variation and using data to quantify variation and measure effects in order to improve processes. It also discusses how statistical thinking can be applied at different levels from executives to managers to workers.
Paper Presnetation on ISO/IEC 17025:2017 organized at Labtech2017 in Bahrain. The topics discussed in that presentation like what are the major changes, what is considered in revised ISO 17025:2017, requirements of ISO 17025:2017, etc. are explained in this ppt presentation.
This document provides guidelines on documented information as required by ISO 9001:2015. It defines documented information as information that must be controlled and maintained, and can be in any format or medium. Documented information serves several objectives including communication, providing evidence of conformity, knowledge sharing, and preserving organizational experiences. Both documents required for the quality management system and those necessary for effective operations must be maintained. Records are a type of documented information needed to provide evidence of results achieved and must be retained. The document lists numerous examples of the types of records required by different clauses of ISO 9001:2015.
This document summarizes an email from i-Sight promoting their case management software. It thanks the reader for downloading a CAPA template, and explains that i-Sight's software provides a robust online platform for organizing documents, forms, and evidence related to nonconformances and the CAPA process. The software offers features like alerts, centralized access, task management, and real-time dashboards. It encourages the reader to book a demo to learn how i-Sight can help manage their business's CAPA processes.
The document summarizes revisions made to ISO/IEC 17025:2017, the standard for testing and calibration laboratories. Key changes include:
- Aligning the structure and language with other ISO standards and emphasizing outcomes over prescriptive requirements.
- Adding definitions for terms like "intralaboratory comparison" and updating terms like "impartiality".
- Focusing on risk-based thinking and giving laboratories more flexibility in meeting requirements.
- Emphasizing process approaches and addressing new areas like information technology and electronic documents.
- Providing two options for management system requirements - addressing specific clauses or using ISO 9001:2015.
The document discusses the process for updating an existing ISO/IEC 17025:2005 accredited laboratory management system to comply with the revised ISO/IEC 17025:2017 standard. It outlines 8 key steps, including conducting awareness training on the revisions, reviewing and revising documentation, implementing risk-based thinking, training auditors, conducting internal audits, addressing nonconformities, applying for an updated accreditation certificate, and undergoing a final assessment audit. Accredited laboratories must complete the upgrade process within 3 years of the 2017 standard's release.
Paper Presnetation on ISO/IEC 17025:2017 organized at Labtech2017 in Bahrain. The topics discussed in that presentation like what are the major changes, what is considered in revised ISO 17025:2017, requirements of ISO 17025:2017, etc. are explained in this ppt presentation.
This document provides guidelines on documented information as required by ISO 9001:2015. It defines documented information as information that must be controlled and maintained, and can be in any format or medium. Documented information serves several objectives including communication, providing evidence of conformity, knowledge sharing, and preserving organizational experiences. Both documents required for the quality management system and those necessary for effective operations must be maintained. Records are a type of documented information needed to provide evidence of results achieved and must be retained. The document lists numerous examples of the types of records required by different clauses of ISO 9001:2015.
This document summarizes an email from i-Sight promoting their case management software. It thanks the reader for downloading a CAPA template, and explains that i-Sight's software provides a robust online platform for organizing documents, forms, and evidence related to nonconformances and the CAPA process. The software offers features like alerts, centralized access, task management, and real-time dashboards. It encourages the reader to book a demo to learn how i-Sight can help manage their business's CAPA processes.
The document summarizes revisions made to ISO/IEC 17025:2017, the standard for testing and calibration laboratories. Key changes include:
- Aligning the structure and language with other ISO standards and emphasizing outcomes over prescriptive requirements.
- Adding definitions for terms like "intralaboratory comparison" and updating terms like "impartiality".
- Focusing on risk-based thinking and giving laboratories more flexibility in meeting requirements.
- Emphasizing process approaches and addressing new areas like information technology and electronic documents.
- Providing two options for management system requirements - addressing specific clauses or using ISO 9001:2015.
The document discusses the process for updating an existing ISO/IEC 17025:2005 accredited laboratory management system to comply with the revised ISO/IEC 17025:2017 standard. It outlines 8 key steps, including conducting awareness training on the revisions, reviewing and revising documentation, implementing risk-based thinking, training auditors, conducting internal audits, addressing nonconformities, applying for an updated accreditation certificate, and undergoing a final assessment audit. Accredited laboratories must complete the upgrade process within 3 years of the 2017 standard's release.
Premises should be located, designed, constructed and utilized.
Premises design recommendations are described in these guidelines. Design decisions should be based on the type of cosmetic product produced, existing conditions, cleaning and, if necessary, sanitizing measures used.
ISO22716廠房設施可依貴公司生產的化妝品類別,環境現況等設計規劃,確保生產環境的清潔與消毒,應為化妝品廠重要的功課
ISO22716 Cosmetics -- Good Manufacturing Practices (GMP) -- Guidelines on Good Manufacturing Practices,全球通用標準
GMPC歐盟稱 Guideline for Good Manufacture Practice of Cosmetic Products,歐盟成員承認
美FDA稱Cosmetic Good Manufacturing Practices Guidelines,美國承認
屬區域標準