The days of maintaining paper records across the life sciences development and production pipeline are gone. Today’s regulatory requirements, not to mention the complexity of new treatments, requires organization that can only be provided electronically. However,...
Making Medicine Personal with Flexible Automation Solutions
Personalized medicine manufacturers are rapidly changing their manufacturing platforms to provide a new scale of production. In the Emerson Exchange Virtual Series, life sciences experts held an open Q&A on the trajectory of cell and gene therapies, and how a...
Electronic Batch Record Design Considerations
Last week, the 2nd International Summit on GMP, GCP & Quality Control was held in Chicago, Illinois USA. Emerson's Heather Schwalje, a senior Life Sciences consultant, presented Moving beyond part 11; Quality assurance considerations for translating Current Good...
Paperless, Release by Exception Electronic Workflows
If your current work processes are causing delays in getting your manufactured products released for sale, you may want to catch Christie Deitz', Electronic Workflow for a Bioreactor presentation. She'll be co-presenting with an automation engineer from a leading...
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