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      WEBINAR:  Tuesday, August 22, 2017



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Are you anxious that your upcoming Health Authority Inspection will bring more CAPAs?

Your organization spends a considerable amount of effort and resources on processing pharmacovigilance cases and generating Aggregate Reports — but you’re still not sure inspectors will be convinced your PV operational oversight is truly adequate. Ever wonder what it would be like to go into an inspection confident that you knew the status of your AEs and Aggregate Reports? Or that you could get out in front of potential problems regulators might uncover?

See how one organization realized it needed to transcend the focus on individual AE case processing and Aggregate Report Tracking to gain visibility of the whole PV landscape. With changes in regulations and increased demands on patient safety, stress within corporate pharmacovigilance, clinical development, and post-marketing groups are at an all-time high.

This pharmacovigilance webinar will demonstrate proactive approaches to reduce late cases and aggregate reports, increase quality and compliance oversight in all areas of pharmacovigilance, leading to fewer and more effective CAPAs and improved health authority inspection readiness.

Please click here to register and join us for a free webinar on Tuesday, August 22nd at 12:00pm EDT.