Transform Your Approach To Pharmacovigilance and Medical Information
One of the biggest challenges when it comes to pharmacovigilance (PV) and medical information services (MI) is the huge time and cost required to maintain PV and MI in every country where clients manufacture and sell products.
Variations in language, process and privacy regulations cause pharmaceutical companies to maintain dedicated PV teams in each location. This has previously allowed companies to try and ensure a localized approach to translating adverse event (AE) documents, handling inquiries, and additional responsibilities such as local QPPV, local aggregate reporting, local literature review, etc.
It is an inefficient process, which biopharma companies have struggled with for years. In this webinar, experts discuss how to act locally while thinking globally to:
• Enhance oversight of local affiliates/local operating companies
• Improve efficiency and drive cost savings with an optimized structure for local activities
• Increase patient safety through process standardization
• Mitigate strains on local country teams from volume variations
Speakers:
Alisa Hummings
Global Head, Medical Information and Local AE Intake,
IQVIA
Alisa Hummings joined IQVIA in 2010 and provides global leadership of the Medical Information and Local AE Intake Department. Alisa is responsible for global oversight and strategic leadership, and ensures proper governance is in place for all programs with Medical Information and AE Intake scopes.
Located in RTP, North Carolina, Alisa has over 24 years of management experience and 17 years of CRO, pharmacovigilance, and medical affairs expertise.
Barry Mulchrone
Head of Pharmacovigilance Oversight and Analytics,
IQVIA
Barry Mulchrone leads IQVIA’s department responsible for periodic safety reports, risk management solutions, signal management, pharmacovigilance agreements and Qualified Persons for Pharmacovigilance (QPPV). Barry also provides strategic leadership and oversight for major accounts within IQVIA Lifecycle Safety.
Located in Dublin, Ireland, Barry has over 18 years of experience in pharmacovigilance and risk management and has operated as an EU Qualified Person for Pharmacovigilance.
Hosted by
Lori Ellis
Custom Content Writer
Pharma Intelligence
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