Applicable Standard to Laboratory Management

Request a ISO 17025 Guideline document

   ISO 17025       iso 17025 certification quotation-request, ISO 9001 14001 27001 22000 13485 ohsas 18001 nabh nabl certification, training, implementation, certificate manual. ISO certification in Ahmedabad, Baroda,  Rajkot, Surat, Vaapi, Ankleshwar, Mumbai Bombay, Pune, Bangalore, Maharashtra, Gujarat, India USA, Canada, Europe, U.K., Europe, Asia & Africa, China Guideline

There are two main sections in ISO/IEC 17025 - Management Requirements and Technical Requirements. Management requirements are primarily related to the operation and effectiveness of the quality management system within the laboratory. Technical requirements address the competence of staff, methodology and test/calibration equipment.

Laboratories use ISO/IEC 17025 to implement a quality system aimed at improving their ability to consistently produce valid. It is also the basis for accreditation from an Accreditation Body. Since the standard is about competence, accreditation is simply formal recognition of a demonstration of that competence.

A prerequisite for a laboratory to become accredited is to have a documented quality management system. The usual contents of the quality manual follow the outline of the ISO/IEC 17025 standard.

The standards ISO 17025 comprises two parts:

  • Part 1, the Code of Practice, provides BCM best practice recommendations. Please note that this is a guidance document only.
  • Part 2, the Specification, provides the requirements for a Business Continuity Management System (BCMS) based on BCM best practice. This is the part of the standard that you can use to demonstrate compliance via an auditing and certification process.

Being independently certified to the ISO 17025 Part 2 by BSI Management Systems, an independent third-party will be the ultimate assurance to your stakeholders that you comply with BCM best practice.


Benefits
ISO 17025 implementation improves / leads to

  • POLICIES & OBJECTIVES set by 'top management'
  • Conformance to Legal and Regulatory Requirements
  • Recognition by regulators around the world of ISO 17025 as a good basis for addressing medical device design and manufacturing regulatory requirements
  • Controlled consistency of manufactured products
  • Managed productivity and efficiency, controlling costs
  • Competitive advantage and increased marketing and sales opportunities.
  • Improved customer perception of the organization's image, culture and performance.
  • improved internal and external Communications
  • greater understanding of the organization's processes
  • clear responsibilities and authorities agreed for all staff
  • improved use of time and resources
  • reduced wastage
  • greater consistency and traceability of products and services
  • Customer Confidence, Satisfaction and TRUST
  • Level of Assurance in Organisational QUALITY
  • Organisational PROFITABILITY
  • Ability to Differentiate Organisation for Competitive Advantage
  • Organisational Credibility & Reputation

Training
We offer a customized training programme on ISO 17025 for

Next Applicable Standard:  ISO 17025
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Other Applicable Standards
ISO 9001, ISO 29001, API.

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