on 11-10-2009 8:35 AM
Hi, dear QM masters!
May anyone help me with answer of this question:
Are the under-mentionned assumptions standard for the SAP QM module:
For testing delivered materials:
- Description of methods and tests for the trials done, according to the existing standards
- Description of the standard values and/or standard limits of the results for given tests of the tested materials
- Comparison of the real test results with given standards and issuing of document for acceptong delivery (visa) or document for stating that given parameter is outside the standard limits. The documents sholud be according to ISO 9001-2004.
- Reports generation for all results/data, based on different parameters
For testing own production:
- Assigning individual number and/or batch of the produced materials
- Description of specifocations /type of laboratory control/ with possibility for validation
- Description of different testing methods, according to ISO 9001-2004
- Description of given tests with given attributes
- Possibility to enter a result for given batch, for given test, for given trial, according to given method in a given specification/laboratory
Thank you very much in advance!
thank you!
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Dear Katia
your understanding is correct. these assumption can be brought into reality through SAP QM .
SAP QM suffices the ISO requirement and in some cases you need to tailor according to your need
Regards
Gajesh
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hi
I don't know about the assumption or what this data (& from where it reflect from?) but
I can tel you whether following is possible through std QM
For testing delivered materials:
- Description of methods and tests for the trials done, according to the existing standards:YES by DMS or Inspection method in task list MIC's
- Description of the standard values and/or standard limits of the results for given tests of the tested materials:YES by inspection method & MIC
- Comparison of the real test results with given standards and issuing of document for acceptong delivery (visa) or document for stating that given parameter is outside the standard limits. The documents sholud be according to ISO 9001-2004.: No
- Reports generation for all results/data, based on different parameters: yes by Inspection results after Result recording
For testing own production:
- Assigning individual number and/or batch of the produced materials: Yes
- Description of specifocations /type of laboratory control/ with possibility for validation :YES by DMS or Inspection method in task list MIC's
- Description of different testing methods, according to ISO 9001-2004:YES by inspection method & MIC
- Description of given tests with given attributes: yes DMS
- Possibility to enter a result for given batch, for given test, for given trial, according to given method in a given specification/laboratory:Yes,standard RR
Regards
Sujit
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