ISO 17034 2016 パッケージ
$589
- 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
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.
- 環境 and specialized equipment .
- Requirements for organization and ドキュメンテーション.
- 対策 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 品質管理体制 that ensures compliance with the laboratory’s internal documentation procedures.
- Adaptability to changes in the technical or organizational framework of the laboratory .
- コントロールズ 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 規格
- Continuously improve the quality management system and testing/calibration practices.
3????? ISO 17034 2016 Package
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このパッケージは、同じ会社で働くすべての人が、役職や部署に関係なく利用することができます。プロセスや手続きの合理化を支援すると同時に、生産性と効率性を高めるための包括的なソリューション・スイートを提供します。このパッケージでは、最大50人のユーザーがリアルタイムで共同作業を行うことができ、重要なデータを迅速かつ効率的に共有することができます。
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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専門家
こんにちは、すごい人たち!
マリリン・C QSEアカデミーチームより ?.
Marilyn C. は、国際標準化機構(ISO)が定める認定および試験所規格の第一人者です。 ISO 17025、17020、17024、17034、17043の認定について幅広い知識を持つ。 これらの規格に準拠した評価と認証のプロセスを含む。また、ISO9000規格に準拠した品質マネジメントシステム(QMS)の導入にも経験があります。
マリリンは、多くの組織が希望するISOの認定や認証を取得するのを支援してきた、経験豊富なコンサルタントです。ISO や IEC などの国際標準化団体が定める要件を満たすために、プロセスや手順をどのように改善すればよいかを指導しています。また、顧客と密接に連携し、ラボの運用が高い基準を満たし、長期的な成功のために認定を維持できるよう支援します。
さらに、マリリンは以下のようなトレーニングコースも提供しています。 品質マネジメントシステム(QMS)、リスクアセスメント、内部監査 は、ISO 認証取得を目指す人のためのものです。また、このテーマに関する論文をいくつか発表しており、さまざまな業界会議で定期的に講演を行っています。
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.
マリリンは、ISO規格に準拠した研究所の品質管理システムの開発および導入に精通しています。彼女は、次のような能力を備えています。 既存のシステムを見直し、不適合または改善すべき領域を特定する。 さらに、ISOの要求事項や実験室環境での実施方法についての理解を深めるために、スタッフにトレーニングコースを提供することも可能です。
マリリンは、多くの異なる組織の認定プロジェクトに幅広く携わり、国際機関が定めるすべての関連基準を満たすことができるようにしました。また、関連規格への準拠を確認するために、ラボ施設の監査を実施した経験もあります。
この分野の経験豊富なコンサルタントとして、マリリンは、国際規格に完全に準拠するためにどのような変更が必要であるかについて、クライアントにアドバイスを提供することができます。また、ラボラトリーサービスの質を向上させるためのガイダンスや、将来の認証取得に向けた計画も提供します。
? 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.
? Quick links
お問い合わせはこちら https://www.qse-academy.com/contact-us
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? Are you available to discuss how I can get in touch with you?
はい、もちろんです。どのように私に連絡を取っていただけるか、ぜひご相談させてください。私への連絡は、電子メールでお願いします。 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.
ドキュメント
? This package provides you with the following features:
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フル ライフタイム アクセス
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Access on a laptop, desktop, and mobile
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修了証書の発行
? このパッケージの内容
手順
- Procedure for Document Control
- Procedure for Record Control
- Procedure for Management Review
- Procedure for Internal Audit
- Procedure for Corrective Action
- Procedure for Preventive Action
- Procedure for Risk Assessment
- Procedure for Competence, Awareness, and Training
- Procedure for Infrastructure and Work Environment
- Procedure for Monitoring and Measuring
- Procedure for Calibration and Maintenance of Equipment
- Procedure for Purchasing and Supplier Evaluation
- Procedure for Handling Customer Complaints
- Procedure for Design and Development
- Procedure for Production and Service Provision
Records and Forms:
- Document Change Request Form
- Record of Management Review Meeting
- Internal Audit Report Form
- Corrective Action Request Form
- Preventive Action Request Form
- Risk Assessment Register
- Training Needs Analysis Form
- Employee Training Record
- Equipment Maintenance Log
- Supplier Evaluation Record
- Customer Complaint Log
- Design and Development Plan
- Design and Development Review Record
- Production and Service Provision Record
Manual:
- ISO 17034 Quality Manual
Other Documents:
- Organizational Chart
- Process Flowchart
- Job Descriptions
- List of Applicable Legal and Regulatory Requirements
- Quality Policy
- Quality Objectives
- Scope of the Quality Management System
Sops
- SOP for Sample Preparation
- SOP for Reference Material Characterization
- SOP for Reference Material Packaging
- SOP for Reference Material Storage and Distribution
- SOP for Traceability and Uncertainty of Measurement
- SOP for Homogeneity and Stability Testing
- SOP for Interlaboratory Comparisons and Proficiency Testing
- SOP for Confidentiality and Data Security
- SOP for Waste Management and Environmental Safety
パトリック
(??????????)“The quality of the materials included in the ISO Document Kit is top-notch – it has definitely saved me many hours of effort!”
パトリック
(??????????)“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.”
カイ
(??????????)“I’m so glad I chose to use the ISO Documentation Kit for certification – the advice and instructions were invaluable!”