OR WAIT null SECS
Pharmaceutical product labeling is a highly regulated and complex process. A product label is very specific in its content, with respect to safety data, adverse effects and compliance to country specific regulations. Changing regulatory requirements and the number of human resource intensive hand offs makes the process error prone, time consuming and costly – not to mention the risk associated with a bad label. Organizations develop SOPs to streamline processes and enhancing quality; however coupling this with automation systems that eliminate manual intervention is a far superior strategy. We show how automating labeling literature and packaging artwork processes for products through our labeling engine, SciLabel ProTM, delivers global compliance with higher efficiency and quality. SciLabel Prostreamlines and standardizes document, label and artwork content workflow management.