By Anonymous on Friday, May 28, 2004 - 12:06 am:
Hello, everybody
Recently I was asked to submit how I achieved the method what I developed for a compound.
Actually I supposed to do MD on trial and error for column selection and buffer selection in reverse phase.
Can any body suggest How better I have to proceed to give a beutiful report
Thanks
By Anonymous on Friday, May 28, 2004 - 12:28 am:
Read: Snyder, et al. "Practical HPLC Method Development". It is a good source.
By Himika Varma on Wednesday, June 2, 2004 - 04:07 pm:
Go through the USP procedure for Method Development. It is very crisp and clear.
By Anonymous on Wednesday, June 2, 2004 - 05:39 pm:
For pharmaceutical products see ICH Q2A Guideline on Validation of Analytical Procedures: Methodology
http://www.mcclurenet.com/ICHquality.html