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Setting up a Quality control Lab
Our company is planning to set up a Quality control lab for medical textiles. I have been assigned to design it using minimum specifications. I would like to know if there are any guidelines regarding layout and design as suggested by the IEC 17025.
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How training should someone have before they are deemed competent for a specific task?
How training should someone have before they are deemed competent for a specific task?
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ISO 17025 Management document structure
Between Quality Policy and Quality manual which one is superior in the management system document structure
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Questions to check gap analysis to 17025:2017
What Kind of questions should one ask to check gap analysis to 17025:2017 -
Equipment calibration certificate/test report
Please according to iso 17025:2017, who in the laboratory is responsible for:
1- reviewing equipment calibration certificates?
2- signing of test report?
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ISO 17025 in pharmaceutical industry
I would like a brief overview of the linkage of ISO 17025 and GMP -
Expert queries
1) techniques of extracting objective evidence in auditing
2) how to improve on my auditing competency
3) how do you relate ISO 9001 with other quality ISO like ISO 15189:2012? Do i need ISO 9001 to implement ISO 15189:2012?
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Scope of accreditation
The scope of accreditation will fall under which clause of 17025:2017?
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Clause 6.2.2
requirements for education, qualification, training, technical knowledge, skills and experience. what are the meaning of qualification ,experience -
Clause 7.7 7.7.1
The resulting data shall be recorded in such a way that trends are detectable and, where practicable, statistical techniques shall be applied to review the results. This monitoring shall be planned and reviewed and shall include, where appropriate, but not be limited to from (a to K) please can you explain b, c, d, h please can you describe Data from monitoring activities shall be analysed, used to control and, if applicable, improve the laboratory’s activities. If the results of the analysis of data from monitoring activities are found to be outside pre-defined criteria, appropriate action shall be taken to prevent incorrect results from being reported.