In the regulated industries such as pharma and medical devices, recording the data manually is a complex, resource-intensive, and time-consuming process. Therefore, it is essential to switch to automated/computerized systems with dynamic process control, data processing, and data record/storage applications. How can one develop those systems? Read through Freyr’s perspective published in 'Pharmaceutical Online' and 'Bioprocess Online,' authored by Sridhar Sarva, Senior General Manager, specialized in Regulatory and Quality Services.