As QC Laboratory professionals, it is imperative we uphold the highest standards in compliance with Good Manufacturing Practice (GMP). Data integrity is fundamental in a pharmaceutical QC Laboratory quality system which ensures that medicines are of the required quality. A robust data governance system must be designed to ensure QC data is complete, consistent and accurate. The recent high-profile regulatory cases around data integrity in QC Laboratories has highlighted the opportunities to strengthen both paper and computerised elements of the data lifecycle.
In our guide, find out what each of the acronyms in "ALCOA" mean. You will also receive a complimentary pocket guide to easily stick in your lab coat for future use and reference!
