Dear colleagues
Is anyone aware of any regulatory guidelines/information relating to correct document writing or completing. I need to set some rules for completing paperwork to meet FDA expectations. Looking for the basic Do's and Don'ts of completing paperwork.
Any advice is appreciated.
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By Anonymous on Wednesday, August 14, 2002 - 06:14 pm:
If you go to this link and meander through the pages this will hopefully help. http://www.fda.gov/cder/guidance/phase1.pdf
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