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日期: 2026 年 6 月 23 日, 星期二

时间: 9:30am – 4:45pm

地点: Shinagawa, Tokyo

Certainty by Certara provides valuable opportunities to connect you with industry leaders and modeling & simulation (M&S) experts. Certara’s experts and guest speakers present the latest regulatory updates, applied case studies, and the cutting-edge technologies including AI/ML related to Model-informed Drug Development, clinical pharmacology, Pharmacometrics, QSP, PBPK, and more.​​

As a new feature in 2026, the afternoon agenda will include breakout sessions on (1) Modeling & Simulation Updates and (2) Discovery and Toxicology Assessment. Attendees will select one session during registration.​

We hope this annual event will help you connect with innovative researchers across various pharmaceutical companies and bring the innovations to your team.​

概述

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议程

  • Speakers’ biography (PDF): Coming soon​
  • Timetable with speaker information (PDF): Coming soon​

Morning Plenary Sessions for All Attendees

Global MIDD Regulatory Landscape: FDA & EMA Updates
Modeling & Simulation approaches used for regulatory submissions
QSP latest case studies across all development phases and regulatory
Strategy First: Translational modeling from preclinical to clinical - Case studies of FIH dose justification
Digital Data Flow (DDF) from 3D to 4D

Afternoon Breakout Sessions

Track 1: Modeling & Simulation Updates and Case Studies

MIDD strategies to overcome clinical pharmacology challenges for regulatory approvals - Case studies of dose justification in late phase
[Guest Speaker] Pediatric drug development: current landscape, challenges, and future directions
Chie Emoto, PhD, Chugai Pharmaceutical Co., Ltd/ Laboratory of Drug Metabolism and Pharmacokinetics, Showa Pharmaceutical University
[Guest Speaker] Reaching the Unreached: Accelerating Value Creation in Rare Disease Drug Development Through Australia
Juran Kato, PhD, President & CEO, GEXVal
[Guest Speaker] Regulatory experience with PBPK in DDI evaluation of a novel TROP2-directed antibody-drug conjugate, DATROWAY
Akiko Watanabe, PhD, Daiichi Sankyo
Optimal dosing, optimal outcomes: PBPK case studies for ADCs

Track 2: AI-Enabled Discovery & Candidate Assessment

Enabling AI-driven Modeling and Simulation-based Decision making in Discovery Towards Increased Clinical Drug Candidate Success
Deep Learning in Discovery
安全第一:揭示化合物筛选数据中的临床风险
Why QSP for Drug Discovery - Early feasibility for asset viability
Session for AI-enabled Discovery or Candidate Assessment is coming soon

特邀嘉宾

*Order of presentations

Chie Emoto, PhD

Group Manager of System Pharmacology group, Translational Research Division, Chugai Pharmaceutical Co., Ltd/ Laboratory of Drug Metabolism and Pharmacokinetics, Showa Pharmaceutical University

演讲主题:Pediatric drug development: current landscape, challenges, and future directions

Juran Kato, PhD

President & CEO, GEXVal

演讲主题:Reaching the Unreached: Accelerating value creation in rare disease drug development through Australia

Akiko Watanabe, PhD

Director, Quantitative Clinical Pharmacology Department, Daiichi Sankyo

演讲主题:Regulatory experience with PBPK in DDI evaluation of a novel TROP2-directed antibody-drug conjugate, DATROWAY

Certara’s speakers

Mayumi Hasegawa, PhD

Vice President, Drug Development Solutions, Certara

Noriko Okudaira, PhD

Senior PBPK Consultant, Certara

Josh Apgar
Joshua Apgar, PhD

Vice President, Head of QSP, Certara

Geoff Fatzinger

Vice President, Regulatory Strategy, Certara

Antal Martinecz, PhD

Associate Director, Pharmacometrics, Certara

Felix Stader

Senior Research Scientist, Simcyp Division, Certara

Kate Gill, PhD

Director of PBPK Consultancy, Certara

Nicolas (Nico) Jouven

Global Portfolio Leader, Discovery, Certara

Jiwon Hur, MD

Solutions Consultant, APAC, Certara

Yasuto Nakashima, MS

Senior Solutions Consultant, APAC, Certara

Rico Fujita

​Solution Consultant, Software, Certara

演讲主题:Certara 平台:提升药物研发确定性的先进技术

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