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Labeling Content Management - Clinical, Regulatory Automation solutiLabeling Content Management Big Pharma Challenges Usually, most of the labeling is manual, copy/paste repetitive, manual reconciliations of data points, a lot of QC checklists, and so on Heavily document focused and di
Regulatory Labeling | Freyr - Global Regulatory Solutions and ServicesIn June 2010, The Medicines Control Council (MCC) announced the intention to implement the South African Common Technical Document (ZA CTD) format which will replace the current MRF1 and any applications still in MBR1 fo
Regulatory Publishing: Submission Document ManagementStreamline bio-pharma regulatory operations with automated document publishing, submission management, and regulatory publishing software for compliance.
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