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Virtual Event

2021年9月07日 (火) 午前 8:45 - 2021年9月07日 (火) 午後 5:00

(Singapore Standard Time)

Office No. 250, TImes Square, B Wing, Andheri Kurla Road, Mumbai  400059, India

DIA Asia 2021-The Evolution Of Clinical Trials And Regulatory Science In A Post-Pandemic Digital World In Asia

The timing is as per Singapore Time Zone

Session 3: Digital Technology Advances The Modernization Of Regulatory Science & Drug Development

Session Chair(s)

Fengyun (Vicky)  Han

Fengyun (Vicky) Han

Senior Director, Head of Regulatory Policy for Asia Pacific

Johnson & Johnson Pte. Ltd., Singapore

Rie  Matsui, RPh

Rie Matsui, RPh

Senior Director, Regional Labeling Head for APAC, International Labeling

Pfizer R&D Japan G.K., Japan

Digital is a very dynamic and developing in a very fast manner, it has been wildly applied in almost everywhere and has been accelerated during the COVID-19 pandemic. the pharmaceutical industry and academia have been using many digital tools to accelerate the drug R&D and clinical trial development, and regulator is leveraging the digital technology to improve its drug review and supervision system etc. In this session, will focus on updating of digital technology to advance the regulatory system modernization, and the transitioning to e-labelling by using 2D barcode and structured format, and digital endpoint to facilitating the clinical trial development and cloud based system

Speaker(s)

Tomoko  Ohsawa, PhD

Formal implementation of e-labelling in Japan

Tomoko Ohsawa, PhD

Pharmaceuticals and Medical Devices Agency (PMDA), Japan

Director of Office of Informatics and Management for Safety

Tong  Guo

De-centralised Clinical Trial in China: Progress and Practice

Tong Guo

LinkDoc Technology (Beijing) Co. Ltd, China

Executive Vice President

Kai  Langel

Digital Endpoint Ecosystem & Protocols

Kai Langel

Janssen, Spain

Senior Director, Strategy and Innovation, Global Regulatory Policy

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