S
suka_batang
Due to unavailability and cost of certified reference material (CRM), our laboratory decide to prepare and use in-house reference material (RM) as calibration and verification standards for calibrating/validating our instrument/equipment especially in GC/HPLC/IC.
However,I have some problem when we need to comply with ISO17025
1. Are we require to perform the correction/compensation (actual amount) on the assay/concentration amount of the in-house standards?
2. If yes, there are any tools/methods/templates that more simple & practical which I can use in determine the compensated amount.
3.Then, are the in-house standards also require to have certificate of analysis (COA) and how to report the raw data and result of the compensated amount and what the format the report?
Thanks to all in assist me in this stuff, I'm really need your help.
Thanks
:truce:
However,I have some problem when we need to comply with ISO17025
1. Are we require to perform the correction/compensation (actual amount) on the assay/concentration amount of the in-house standards?
2. If yes, there are any tools/methods/templates that more simple & practical which I can use in determine the compensated amount.
3.Then, are the in-house standards also require to have certificate of analysis (COA) and how to report the raw data and result of the compensated amount and what the format the report?
Thanks to all in assist me in this stuff, I'm really need your help.
Thanks
:truce: