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- Posts: 4
- Joined: Thu May 07, 2009 11:03 pm
In my country a lot of manager of quality and research are working in this problematic situation.
We are writing an article for the official regulatory agency,
about how validate the analytical technics, to pass the problem derived of low acetonitrile disponibility in our country.
The idea is:
To assay and UC, only re-validate these points such as
- Accuracy
- Linearity of accuracy
- Specificity
- All items must pass the system suitability, similar to the original method.
But the problem is the impurities, we are thing only study:
- Linearity
- Lc & LD.
What are we suggest about that? Thanks and sorry for my english
Bye
Ph German Garcia
Quality and Research Manager
Paylos Laboratories SRL