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  1. Good Documentation Practice and Record Keeping Regulations (FDA & EMA)
  2. Developing premarket approval packages for innovations which are more effective in reducing potential adverse events; MAUDES; and or recalls particularly FDA class recalls
  3. Live Webinar FDA’s New Import Program for 2019 : Be Prepared and Be Compliant
  4. Live Webinar 60 minutes Risk Management of Source Water used in the Food Industry