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ISO 17034 2016包装

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  • Increase your credibility in the marketplace by achieving ISO 17034:2016 certification
  • Ensure that your reference materials meet the requirements for homogeneity, stability, identity, and traceability.
  • Complete documentation of ISO 17034 certification requirements and a practical guide to implementation.
  • ➡️All the necessary documents for certification.
  • ➡️ 30-day money-back guarantee.
  • ➡️ Immediate download
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The ISO 17034 document package is designed to help laboratories achieve and maintain performance in accordance with international expectations. It provides guidelines for primary reference material production, quality control, and use, as well as good practices in this area. The documents focus on the identification, marking, and certification of primary reference materials by the responsible organizers.

They also include information on the scientific value of the products and guidance on the appropriate use of primary reference materials to help laboratories achieve and maintain accurate results. ISO 17034 documents are intended for suppliers, customers, and users of primary reference materials to build mutual confidence and improve the quality of results obtained from the use of the materials. They can also help laboratories to meet specific requirements imposed by customers or other entities.

👉What is ISO 17034?

ISO 17034, also known as the “Specifications for the capabilities of laboratories in the management of testing and calibration”, is an international standard that defines the requirements for the quality of the processes and capabilities needed to perform testing and calibration services.

This standard addresses areas such as qualified personnel, working environment, and specialized equipment, as well as organizational and documentation requirements. It also outlines how to maintain and regularly verify proficiency performance, as well as how to ensure a high level of practice that is consistent with the fundamental principles of ISO/IEC 17025.

ISO 17034 also requires an integrated quality management system that ensures that the laboratory’s internal documentation procedures are followed. This system must be adaptable to changes in the technical or organizational environment of the laboratory and include controls over the accreditation and operation of the laboratory. It should provide a complete record of the processes carried out by the laboratory, as well as clear documentary evidence that the technologies used are sufficiently reliable.

👉The requirements of the ISO 17034 standard?

  • Qualified personnel.
  • 环境 and specialized equipment .
  • Requirements for organization and 文件.
  • 措施 to maintain and regularly verify proficiency performance .
  • Ensuring a high level of practice in accordance with the fundamental principles of ISO/IEC 17025 .
  • An integrated 质量管理制度 that ensures compliance with the laboratory’s internal documentation procedures.
  • Adaptability to changes in the technical or organizational framework of the laboratory .
  • 控制措施 over the accreditation and operation of the laboratory.
  • Ability to provide a complete record of the processes performed by the laboratory .
  • Clear documentary evidence that the technologies used are sufficiently reliable

👉This package will help you to

  • Identify, mark, and certify primary reference materials by responsible organizers.
  • Understand the scientific value of products and obtain guidance on the appropriate use of primary reference materials.
  • Assist laboratories in meeting specific requirements imposed by clients or other entities.
  • Ensure a high level of practice in accordance with the fundamental principles of ISO/IEC 17025.
  • Provide a complete record of the processes performed by the laboratory and provide clear documentary evidence that the technologies used are sufficiently reliable.
  • Implement an integrated system that ensures compliance with the laboratory’s internal documentation procedures.

👉 Who this package is for?

  • Organizers responsible for Laboratories that must meet specific requirements imposed by customers or other entities.
  • End users and professionals of primary reference products who are looking for quality certification
  • Industry professionals who want to ensure that their products meet current standards
  • Accreditation bodies, regulatory authorities, and laboratories who want to ensure that their processes comply with ISO 17034 standards
  • Quality- and standards-conscious professionals around the world
  • All organizations seeking internationally recognized certification for their product or service.
  • Individuals interested in continuous improvement of their quality management system and testing/calibration practices.

👉 What are the expected results??

  • Provide quality certification for primary reference material
  • Assist laboratories in meeting specific requirements imposed by clients or other entities
  • Ability to provide a complete record of the processes performed by the laboratory
  • Clear documentary evidence that the technologies used are sufficiently reliable Meet and maintain compliance with industry 标准
  • Continuously improve the quality management system and testing/calibration practices.
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3对ISO 17034 2016 Package的审查

  1. 帕特里克
    (经核实的所有者)

    “The quality of the materials included in the ISO Document Kit is top-notch – it has definitely saved me many hours of effort!”

  2. 帕特里克
    (经核实的所有者)

    “The customer support team that came with my purchase of the ISO Documentation kit was extremely knowledgeable and helpful – they made sure I was able to successfully certify myself on time.”

  3. (经核实的所有者)

    “I’m so glad I chose to use the ISO Documentation Kit for certification – the advice and instructions were invaluable!”

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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在认证和标准方面的专业知识使她成为任何希望达到国际卓越标准的实验室或组织的宝贵财富。她对质量和客户服务的承诺确保客户在与Marilyn C.合作时得到最好的结果,使她成为寻求ISO认证或QMS指导的人的最佳选择。

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。

👉 QSE学院背后是谁?

QSE学院是一个由独立的ISO顾问组成的小团队,在世界各地工作。我们的团队致力于提供一流的质量和环境标准咨询服务,帮助企业充分发挥其潜力。我们努力根据每个客户的需求提供个性化的、具有成本效益的服务。我们的顾问在ISO 9001、14001和45001领域拥有众多认证,使他们有能力应对任何质量或环境挑战。在QSE学院,我们热衷于帮助企业成长和成功,为他们提供实现目标所需的工具。我们的团队致力于提供全面的咨询服务,为每个客户的独特业务需求量身定做。我们努力通过提供一流的服务和支持,确保我们的客户从他们的投资中获得最大收益。凭借在质量、环境和安全标准咨询方面的多年经验,我们将确保你达到你所期望的成功水平。我们期待着与您合作。

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👉 你是否可以讨论我如何与你联系?

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.我每天会多次检查我的电子邮件,通常在24小时内回复,所以这是与我联系的最快方式。更重要的是,你还会有24/7全天候的聊天支持。

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文件

👉这个软件包为你提供了以下功能。

  • 全程 终生 访问
  • Access on a laptop, desktop, and mobile
  • 结业证书

👉 本套餐包括

程序。

  1. Procedure for Document Control
  2. Procedure for Record Control
  3. Procedure for Management Review
  4. Procedure for Internal Audit
  5. Procedure for Corrective Action
  6. Procedure for Preventive Action
  7. Procedure for Risk Assessment
  8. Procedure for Competence, Awareness, and Training
  9. Procedure for Infrastructure and Work Environment
  10. Procedure for Monitoring and Measuring
  11. Procedure for Calibration and Maintenance of Equipment
  12. Procedure for Purchasing and Supplier Evaluation
  13. Procedure for Handling Customer Complaints
  14. Procedure for Design and Development
  15. Procedure for Production and Service Provision

Records and Forms:

  1. Document Change Request Form
  2. Record of Management Review Meeting
  3. Internal Audit Report Form
  4. Corrective Action Request Form
  5. Preventive Action Request Form
  6. Risk Assessment Register
  7. Training Needs Analysis Form
  8. Employee Training Record
  9. Equipment Maintenance Log
  10. Supplier Evaluation Record
  11. Customer Complaint Log
  12. Design and Development Plan
  13. Design and Development Review Record
  14. Production and Service Provision Record

Manual:

  1. ISO 17034 Quality Manual

Other Documents:

  1. Organizational Chart
  2. Process Flowchart
  3. Job Descriptions
  4. List of Applicable Legal and Regulatory Requirements
  5. Quality Policy
  6. Quality Objectives
  7. Scope of the Quality Management System

Sops

  1. SOP for Sample Preparation
  2. SOP for Reference Material Characterization
  3. SOP for Reference Material Packaging
  4. SOP for Reference Material Storage and Distribution
  5. SOP for Traceability and Uncertainty of Measurement
  6. SOP for Homogeneity and Stability Testing
  7. SOP for Interlaboratory Comparisons and Proficiency Testing
  8. SOP for Confidentiality and Data Security
  9. SOP for Waste Management and Environmental Safety
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