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Management systems requirements

Environmental management system requirements 4.1 General requirements... [Pg.542]

Auditing While inspection verifies the condition of equipment, auditing verifies procedural and management system requirements. Installation now should focus on existing systems. Other audit elements can be added later. j... [Pg.93]

The International Standard, ISO 9001 2000, Quality Management Systems -Requirements, is a general standard that applies to all types of organizations,... [Pg.15]

Quality Management Systems - Requirements , ISO 9001 2000, International Organization for Standardization (ISO), Geneva, Switzerland, 2000. [Pg.24]

As has already been mentioned in Chapter 2, ISO 9001, Management Systems - Requirements , is increasingly being adopted by laboratories to cover the aspects of their business that are not laboratory based. This is because this Standard is more about controlling the process and service enhancement rather than technical issues. It requires continuous improvement, demonstrating that quality is not a static process. The requirements for such matters as documentation, document control, purchasing and management responsibilities are much the... [Pg.228]

The laboratoiy quality manual is a document addressing the quality management system requirements and shall... [Pg.48]

The monitoring of the laboratory performance is required to demonstrate that the laboratory product conforms to the specified requirements and that the laboratory activity conforms to the quality management system requirements. Moreover, there is a need and it is a requirement that the laboratory continually improves the effectiveness of the quality management system. [Pg.65]

A laboratory s fulfillment of the requirements of ISO/IEC 17025 2005 means the laboratory meets both the technical competence requirements and management system requirements that are necessary for it to consistently deliver technically competent test results and calibrations... [Pg.92]

Furthermore, the equivalence in the way both the laboratoiy accreditation standard and the certification standard deal with the management system requirements illustrates that an accredited laboratory meets, in practice, these requirements as specified in ISO 9001. After a proposal made via Eurachem and EA to ILAC, a similar joint Communique was agreed and signed in September 2009 by ILAC, lAF and ISO for medical laboratories against ISO 15189 2007. [Pg.92]

The management system requirements In ISO/IEC 17025 2005 (Section 4) are written in language relevant to laboratory operations and meet the principles of ISO 9001 2000 Quality management systems -Requirements and are aligned with its pertinent requirements . [Pg.92]

American National Standards Institute (ANSI) (2000), Quality management system— Requirements, ANSI/ISO/ASQ Q9001-2000, ANSI, New York. [Pg.237]

ISO (2000), Quality management systems—Requirements, 9001 3rd ed. (Geneva International Organization for Standardization). [Pg.284]

Fraser CG, Kallner A, Kenny D, Peterson PH (1999) Strategies to set global analytical quality applications in laboratory medicine. Scand J Clin Lab Invest 59 477-478 IS09001 2000 Quality management systems - Requirements. International Organization for Standardization (ISO), 1, Rue de Varentie, Case Postals 56, CH-2111 Geneva 20, Switzerland... [Pg.24]

Requirements for the qualification of personnel and quality management system requirements... [Pg.94]

Conforms to the planned arrangements (see 7.1), the requirements of the international standards, and the quality management system requirements established by the organization... [Pg.107]

ISO 9001 1994, Quality System — Model for Quality Assurance in Design, Development, Production, Installation, and Servicing ISO 9001 2000, Quality Management System Requirements. Design, Manufacture, and Final Product Inspection and Testing. [Pg.126]

Documentation plays an important role in the effective control and implementation of quality management system requirements. The quality policy, objective, and applicable procedures ensure to meet ... [Pg.278]

The quality-related material requisitions are raised with material specification, describing code number, and subjective and quantitative details. Purchasing information describes the product to be purchased, including, where appropriate, requirements for approval of product, procedures, processes and equipment, requirements for qualification of personnel, and quality management system requirements. [Pg.348]

ISO 10012, 2003. Measurement management systems - Requirements for measurement processes and measuring equipment. [Pg.26]

The pharmaceutical manufacturer s quality management system requirements are met at all stages of the project. [Pg.582]

See other pages where Management systems requirements is mentioned: [Pg.170]    [Pg.83]    [Pg.170]    [Pg.231]    [Pg.52]    [Pg.77]    [Pg.542]    [Pg.33]    [Pg.216]    [Pg.42]    [Pg.17]    [Pg.71]    [Pg.93]    [Pg.93]    [Pg.93]    [Pg.159]    [Pg.283]    [Pg.236]    [Pg.190]    [Pg.252]    [Pg.433]    [Pg.26]    [Pg.869]    [Pg.412]    [Pg.513]   
See also in sourсe #XX -- [ Pg.160 ]



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