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Jim Cahill
21 Nov 2013
GMP requirement
biotech manufacturing
EBR
Life Sciences
ISA/ANSI-95
CGMP
ISA-95
Operations Management
Heather Schwalje
S-95
electronic batch record
current good manufacturing practices
pharmaceutical manufacturing
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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...
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