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Organiser: Lumanity

Speaker(s): Abigail Postema, MPhil & Premysl Velek, MSc

Moderator: Deborah Layton, PhD

While evidence triangulation and complementary analytical methods are well established, there is much less discussion about how they should be integrated and interpreted as a coherent body of evidence.

Using practical examples from vaccine safety and comparative effectiveness research, this webinar will explore the challenge of causal evidence triangulation for pharmacoepidemiology. Specifically, how combining complementary study designs and targeted sensitivity analyses produces robust, regulator-ready causal interpretations in drug safety and efficacy studies.

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