01.22.13 -- Advanced Incubation Solution For Cell-Based Research
Basics Of Labwasher Cleaning Validation A Q&A with James Espiritu, Miele
Validation is vital to pharmaceutical processes because it assures quality, consistency, and keeps your operations compliant with GMPs. The FDA provides guidance for proper cleaning validation, however challenges occur because interpretation of those procedures vary between facilities.
Tecan and HP have teamed up to reinvent the drug titration process for small molecules by providing a solution which eliminates the traditional serial dilution process, going from concept to experiment to results much faster and giving access to compound studies that were previously impractical.
Before global cleanroom classifications and standards were adopted by the ISO, the U.S. General Service Administration's standards were applied virtually worldwide. However, as the need for international standards grew, the ISO established a technical committee and several working groups to delineate its own set of standards.