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  1. 4-Hour Virtual Seminar - Batch Record Review and Product Release
  2. 6-Hour Webinar 21 CFR Part 11 (Electronic Records/Electronic Signatures) Compliance for Computer Systems Regulated by FDA
  3. 21 CFR Part 11, SaaS/Cloud, EU GDPR Live Webinar
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  5. 90 Minutes Live Webinar Quality Management and Quality Audit According to GxP/GMP Requirements