Hi Everyone in Histoland! Happy Hump day! I have 2 questions to ask you. The CAP "#ANP.21382 Reagent Expiration Date", Evidence of compliance requires a written policy for evaluating reagents lacking manufacturer's expiration date.
I worked in the Biotech arena for several years in R&D and manufacturing. We had procedures which were in compliance to GLP and manufacturing standards. These policies were much more rigid than for AP departments, who adher to CAP requirements. Would any of you kind people like to share a copy of your written policy with me. I would be forever grateful! Second question: How do you address powder dyes, and chemicals in crystalin and powder form, which are extremely old and do not have an expiration date? What is your criteria for passing of failing these chemicals and dyes? Do you visually inspect these chemicals and dyes on an annual basis, and if they look fine, give it another year for a visual check with next years date, or do you send them out to a company for analysis to see if they past required specifications??? That would be pretty costly! If anyone has a written procedure for this I would love to see it too! Thank you in advance for your assistance. Akemi Akemi Allison BS, HT(ASCP)HTL E-Mail: akemiat3...@yahoo.com _______________________________________________ Histonet mailing list Histonet@lists.utsouthwestern.edu http://lists.utsouthwestern.edu/mailman/listinfo/histonet
