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 Manufacturing Practices (cGMP) compliance into Electronic Batch Record (eBR) initiatives. Her discussion centered around three areas: eBR […]
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 pharmaceutical manufacturer at the 2010 World Batch Forum North American Conference, which will be held May […]
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