ISO 17020 2012包装
$589
- Enhance your reputation, reliability, and credibility in the marketplace.
- Increase client confidence that your inspections are performed accurately and reliably
- Complete documentation of ISO 17020 accreditation requirements and a practical guide to its implementation.
- ??All documents required for accreditation.
- ?? 30-day money-back guarantee.
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? What is ISO 17020 2012?
ISO 17020:2012 规定了对进行检查的机构的能力以及其检查活动的公正性和一致性的要求。
它适用于所有作为检验机构或校准实验室开展检验和/或校准活动的组织，无论其法律形式如何。
ISO 17020 2012 is intended to be used by accreditation bodies in the assessment and recognition of conformity assessment bodies (inspection and calibration laboratories). It is also intended to be used by organizations or bodies that certify or otherwise recognize such conformity assessment bodies. ISO 17020 2012 describes the general requirements for the competence, impartiality, and consistency of inspection activities. It covers areas such as management systems, personnel qualifications and training, calibration, sampling plans, and reporting of results.
此外，它还涵盖了与技术能力评价（如检验人员的资格）和其他形式的保证有关的方面，如认证、同行评审和自我评估。
其目的是确保以一致和系统的方式进行检查，在整个过程中采用适当的方法和程序。
The standard provides guidance on how an organization can fulfill its obligations in order to meet the requirements of ISO 17020 2012.
It also provides information on how to monitor and assess an organization?s performance in meeting these requirements.
该标准旨在供所有开展检查或校准活动的组织使用，无论其规模或类型如何。
Additionally, it helps to protect against potential liabilities resulting from incorrect or inconsistent assessment results. The standard also provides guidance on methods and procedures that should be used when conducting inspection activities, helping to ensure consistency and accuracy of results across all organization?s operations. ISO 17020 2012 is an important standard and should be consulted by organizations wishing to ensure the highest levels of quality and customer satisfaction when carrying out inspection activities.
? What contains this ISO 17020 2012 Package:
ǞǞǞ ISO/IEC 17020:2012 一揽子计划包含各种文件和材料，以帮助组织满足标准中规定的要求。它包括对管理系统、人员资格和培训、校准、采样计划和结果报告的指导。
此外，它还就如何评价技术能力和其他形式的保证，如认证、同行评审和自我评估提供了指导。
这套资料还包括如何根据这些要求监测组织绩效的信息。
这套文件包括详细的指导方针，以便在所有业务中以一致和准确的方式进行检查。
The documents in the ISO/IEC 17020 2012 Package aim to ensure that organizations have the necessary procedures and protocols in place for conducting inspections. 这些文件中涉及的具体主题包括：检查范围和目标；人员资格、培训和评估；设备校准；检查计划的制定；数据收集方法；报告撰写指南；风险评估过程；样本选择标准；与检查活动有关的内部审计活动；确保检查结果公正性和一致性的质量控制措施；对根据检查过程中发现的不符合项采取的纠正措施进行核查；与纠正措施实施监测有关的后续活动；认证要求；以及文件控制过程。
?Who this Package is for:
本ISO/IEC 17020:2012包是各行业负责检查活动的组织的重要资源。需要确保其检查以一致、准确和公正的方式进行的公司可以使用它。这套资料为如何评估技术能力和其他形式的保证提供了指导，如认证、同行评审和自我评估。它对那些需要遵守ISO/IEC 17020:2012以满足法律或监管要求的公司特别有用。这套教材对于参与产品和服务检验的组织来说是必不可少的。
?What are the anticipated outcomes?
该ISO/IEC 17020:2012包的预期结果是提高客户满意度和加强质量控制。通过对管理系统、人员资格和培训、校准、抽样计划、报告编写指南和其他领域的指导，该包帮助各组织确保其检查以一致和可靠的方式进行。
2?ISO 17020 2012 Package???
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这个软件包可以被所有在同一公司工作的人使用，无论他们的职位或部门。它提供了一套全面的解决方案，帮助简化流程和程序，同时提高生产力和效率。有了这个软件包，多达50个用户可以实时合作，使他们能够快速有效地分享重要数据。
Yes, there are versions of the package available in several other languages. In addition to Italian, German, Portuguese, Swedish, and Japanese, Chinese is also offered. For those looking to use the package in a language other than English, this gives them a great option. If you have any queries, please contact us on the chat or send an email to support@qse-academy.com
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专家
你好，了不起的人们
Marilyn C. 来自QSE学院团队.
Marilyn C. 是国际标准化组织（ISO）规定的认证和实验室标准方面的主要专家。 她对ISO 17025、17020、17024、17034和17043认证有广泛的了解。 包括根据这些标准的评估和认证过程。她还拥有实施符合ISO 9000标准的质量管理体系（QMS）的经验。
Marilyn是一位经验丰富的顾问，她已经帮助许多组织实现了他们期望的ISO认证或证书。她就如何改进流程和程序提供指导，以满足ISO和IEC等国际标准机构提出的要求。她与客户紧密合作，确保实验室的运作符合这些高标准，以便他们能够保持他们的认证，获得长期成功。
此外，Marilyn还提供以下培训课程 质量管理系统（QMS）、风险评估和内部审计 为那些希望追求ISO认证的人提供服务。她还发表了几篇关于该主题的论文，并经常在各种行业会议上发言。
Marilyn?s expertise in accreditations and standards makes her an invaluable asset to any lab or organization looking to meet international standards of excellence. Her commitment to quality and customer service ensures that clients receive the best possible results when working with Marilyn C., making her an excellent choice for those seeking ISO certification or QMS guidance.
Marilyn精通于为实验室制定和实施符合ISO标准的质量管理体系。她有能力 审查现有系统，并确定不符合要求或需要改进的地方。 此外，她有能力为员工提供培训课程，以提高他们对ISO要求的理解，以及如何在实验室环境中实施这些要求。
Marilyn曾与许多不同的组织在认证项目上广泛合作，确保他们能够满足国际机构规定的所有相关标准。她还拥有对实验室设施进行审计的经验，以检查是否符合相关标准。
作为该领域经验丰富的顾问，Marilyn可以为客户提供建议，说明需要做出哪些改变以确保完全符合国际标准。她可以为提高实验室服务质量提供指导，并为未来的认证制定计划。
? Who?s behind QSE Academy?
QSE Academy is a small team of independent ISO consultants working from all around the world. Our team is dedicated to providing best-in-class quality and environmental standards consulting services that help businesses reach their full potential. We strive to provide personalized, cost-effective services tailored to each client’s needs. Our consultants hold numerous certifications in the fields of ISO 9001, 14001, and 45001, making them well-equipped to meet any quality or environmental challenge. At QSE Academy, we?re passionate about helping businesses grow and succeed by providing the tools they need to reach their goals. Our team is committed to offering comprehensive consulting services that are tailored to each client’s unique business needs. We strive to make sure our clients get the most out of their investments by providing top-notch service and support. With years of experience in quality, environmental, and safety standards consulting, we?re here to ensure that you reach your desired level of success. We look forward to working with you.
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是的，当然。我很乐意讨论你如何与我取得联系。联系我的最佳方式是通过电子邮件，地址是 Support@qse-academy.com. I check my emails multiple times a day and typically respond within 24 hours so that’s the quickest way to get in touch with me. What’s more, you’ll also have 24/7 chat support around the clock.
文件
? This package provides you with the following features:
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全程 终生 访问
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Access on a laptop, desktop, and mobile
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结业证书
? 本套餐包括
Manual:
- ISO 17020 Quality Manual
程序。
- Control of Documents Procedure
- Control of Records Procedure
- Internal Audit Procedure
- Management Review Procedure
- Corrective Action Procedure
- Preventive Action Procedure
- Control of Nonconforming Services Procedure
- Competence and Training Procedure
- Inspection Procedure
- Equipment Calibration and Maintenance Procedure
- Complaints Handling Procedure
- Confidentiality and Impartiality Procedure
- Contract Review Procedure
- Purchasing and Supplier Evaluation Procedure
- Risk Management Procedure
Records and Forms:
- Document Change Request Form
- Master Document List
- Record Retention Schedule
- Internal Audit Report
- Internal Audit Checklist
- Management Review Minutes
- Corrective Action Report
- Preventive Action Report
- Nonconforming Services Report
- Employee Training Record
- Competency Assessment Form
- Inspection Report
- Calibration Certificate
- Equipment Maintenance Log
- Complaint Register
- Confidentiality Agreement
- Impartiality Declaration
- Contract Review Checklist
- Approved Supplier List
- Purchase Order
- Supplier Evaluation Form
- Risk Assessment Matrix
SOPs:
- SOP for Inspection Process
- SOP for Equipment Calibration and Maintenance
- SOP for Complaints Handling
- SOP for Confidentiality and Impartiality
- SOP for Contract Review
- SOP for Purchasing and Supplier Evaluation
- SOP for Risk Management
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凯文
(???????)-This template is an invaluable tool for any organization looking to become ISO certified and stay compliant with their own corporate policies as well as international standards.
诺兰
(???????)– Ultimately, the use of this template will enable an organization to confidently meet all requirements set by the ISO, ensuring that they remain compliant both domestically and internationally.