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Monday, June 25 • 2:00pm - 2:30pm
#136: Drug Safety: A Continuum Approach Linking Pre-Market and Post-Market Safety Assessment

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Component Type: Session
Level: Intermediate
CE: IACET 0.50

Seating is limited.
Pharmaceutical Drug Safety is of paramount importance to drug manufacturers, payers, regulators, and the society as a whole as it attracts public attention more so than effectiveness. While there have been significant efforts in monitoring safety thru internal safety groups within the drug manufacturers and independent external committees in the clinical development phase, not a lot of these pre-marketing safety information may be historically translated into a robust pharmacovigilance (PV) and safety monitoring plan in the post-marketing arena. The EMA GVP regulations encourage good PV planning during clinical development but at this stage have not offered recommendations. In order to provide more clarity into potentially suspected safety issues during the clinical trials, follow-up post-marketing real world evidence (RWE) studies could be undertaken. On behalf of the DIA/ASA Biopharm Safety Evaluation Scientific Working Group, currently focusing on safety monitoring during development, it would be important to discuss the possibility of bridging with the post-marketing safety planners in an informal interactive dialogue with subject matter experts in the PV, RWE and Safety area to plan for future collaborations in this important aspect of life-cycle of pharmaceutical drugs.

Learning Objectives

Explain the planning objectives of the ASA Biopharm/DIA Safety Monitoring Assessment Scientific Working Group (SWG); Discuss ways to bridge pre-marketing safety planning recommendations of this SWG to safety planning in post-marketing.

Chair

Susan Duke, MSc


Speakers
avatar for Susan Duke

Susan Duke

Mathematical Statistician, OB, OTS, CDER, FDA
Susan became involved in safety related industry-wide graphics in 2009 when she joined the FDA/Industry/Academia Safety Graphics WG. She is currently a Mathematical Statistician reviewer in CDER and member of a cross-functional safety monitoring WG co-sponsored by DIA and ASA Biopharm... Read More →


Monday June 25, 2018 2:00pm - 2:30pm
Content Hub NE Lobby Boston Convention and Exhibition Center 415 Summer Street, Boston, MA 02210 USA