Date: September 30, 2026
Time: 11:30 AM – 2:00 PM
Location: CIC Cambridge, 1 Broadway, Cambridge, MA 02142
Regulators around the world are converging on the same conclusion: MIDD should be a core part of how evidence is built and evaluated across drug development. ICH M15 has established the first harmonized global framework for MIDD, and FDA’s Operation TrialBlazer guidances, including new recommendations for QSP-based dose selection in first-in-human trials, reflect a broader momentum toward formalizing modeling’s role in regulatory decision-making. Taken together, these developments signal growing confidence in MIDD approaches as trusted contributors to the evidence package, not just supporting analyses.
This session brings together three of Certara’s most recognized scientific leaders across Quantitative Systems Pharmacology (QSP), Physiologically-Based Pharmacokinetics (PBPK), and Pharmacometrics for a candid, cross-disciplinary discussion on this momentum, and how sponsors can capitalize on it by building modeling strategies that give them the best chance of success with regulators.
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Registrations are subject to review and approval

Piet van der Graaf
Senior Vice President and Head of Quantitative Systems PharmacologyPiet van der Graaf, PharmD, PhD is Senior Vice President Applied BioSimulation at Certara, Professor of Systems Pharmacology at Leiden University, and Professor of Pediatrics at Cincinnati Children’s Hospital Medical Center. Previously, he was the Director of the Leiden Academic Centre for Drug Research and held leadership positions at Pfizer in Discovery Biology, DMPK and Clinical Pharmacology. He was the founding Editor-in-Chief of CPT: Pharmacometrics & Systems Pharmacology before becoming Editor-in-Chief of Clinical Pharmacology & Therapeutics. Piet received his doctorate training in clinical medicine with Nobel prize laureate Sir James Black at King’s College London. He was awarded the 2024 Gary Neil Prize for Innovation in Drug Development from the American Society of Clinical Pharmacology and Therapeutics (ASCPT) and the 2021 Leadership Award from the International Society of Pharmacometrics (ISoP). Piet is an elected Fellow of the British Pharmacological Society and has published >250 articles in the area of quantitative pharmacology and drug development.

Karen Rowland Yeo, PhD
Senior Vice President, Client & Regulatory StrategyKaren Rowland-Yeo is Senior Vice President of Client & Regulatory Strategy at Certara UK Ltd. She has over two decades of experience applying PBPK models in both global health and drug development and is currently focused on driving advancement of PBPK modeling in child and maternal health. Prior to her current role, Karen was Head of PBPK Consultancy Services at Certara UK Ltd, where she led a core team of scientists engaged in consultancy projects relating to the application of PBPK modeling in drug development and drove development of best practices while working directly with global regulators to gain acceptance of PBPK models. Karen has authored or co-authored more than 100 publications in peer-reviewed journals spanning clinical pharmacology, drug metabolism, and drug-drug interactions, and is frequently invited to speak at international meetings in the field. In 2023, Karen was awarded the Roger Jelliffe Individualized Therapy Award by the American College of Clinical Pharmacology (ACCP), in recognition of her contributions to personalized medicine through model-informed precision dosing. In 2024, she chaired the Scientific Program Committee for the ASCPT Annual Meeting and served as Deputy Editor-in-Chief of CPT:PSP; in October 2025, she took over the helm as Editor-in-Chief of Clinical Pharmacology & Therapeutics.

Adekemi Taylor, PhD
VP Regional Lead USA, Division 1, Quantitative Science ServicesAdekemi specializes in in pharmacometric strategy and analyses (including population PK, PK/PD, efficacy and safety exposure-response, and concentration-QTc modeling) to support regulatory filings, study design, and general drug development.
Register now
Registrations are subject to review and approval
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