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On Tuesday November 03, 2015 Ashfield Pharmacovigilance will hold a complimentary seminar at the North Carolina Biotechnology Center located at 15 T W Alexander Drive,Durham, NC 27703, USA.

‘Ready, Set, Launch: Is your Pharmacovigilance Plan on Course?’ is designed to enhance the knowledge of pharmaceutical and biotech professionals on the differences in pharmacovigilance requirements when transitioning from clinical to approval stage in a product’s lifecycle or when launching newly acquired products. For more information visit:


A tentative schedule of events is as follows:

8:15am Registration and Networking Breakfast

9:00am Opening Remarks and Introductions

9:15am Pharmacovigilance Approval Checklist for Roles and Resources at Time of Launch

9:45am Reporting Sources for Adverse Events

10:15am Training Your Staff on Adverse Event Responsibilities

10:45am Differences in Clinical and Post Market Medical Review

11:15pm Approvals in Other Countries

11:45pm Lunch

12:45pm Pharmacovigilance Due Diligence for Product Acquisition

1:15pm Market Access Due Diligence for Product Acquisition

1:45pm Closing Remarks

Check what is going on @Ashfield_USA