Overview:

Labs and manufacturing plants strive for operational excellence to reduce development and manufacturing costs, reduce cycle times and at the same improve compliance. Traditionally, the environment has been a hybrid environment of paper and electronic systems—paper notebooks, paper binders and log books—combined with ERP, LIMS, CDS and SDMS systems. More recently this slew of acronyms has been complimented with the Electronic Lab Notebook (ELN). The result is a mixture of informatics products from multiple vendors supporting parts of a process.

In this webinar we will explore the role of these systems in the development and cGMP QA/QC process in leading pharma and biotech companies, and how these systems are evolving and converging to support process efficiency and improved compliance from lab to commercialization that has led to a measured:

• 25% increase in productivity

• 50% reduction in cycle time

• Ten-fold reduction in compliance risk