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Tox Round Table
Advancing drug development through expertise
and innovation in nonclinical research.
Tox Round Table 이란

Introducing the Tox Round Table

Greetings. I am Woo-Chan Son.

Nonclinical development is a field that relies heavily on experience. Even when reviewing the same finding, decisions regarding the threshold for adversity, the establishment of the NOAEL, and the relevance of those decisions to humans cannot be made solely by consulting textbooks and guidelines. Ultimately, people often learn by going through situations that others have already experienced.

The problem is that this hard-earned and valuable experience often remains confined within individuals and companies. In Korea in particular, many drug-development companies are relatively small and may not have dedicated toxicology specialists or may not fully utilize their expertise. The resulting loss of time and resources can be considerable.

Tox Round Table (TRT) is a professional learning community for toxicology practitioners, established in October 2023 to help bridge this gap. It combines ongoing online discussions with regular in-person workshops. Each week, a designated moderator proposes a topic, and members freely ask questions, share perspectives, and exchange practical knowledge.

The community follows three principles. First, there is no participation fee. Second, company confidential information is strictly excluded, and discussions are limited to practical toxicology matters. Third, the quality of a question—not a participant’s title or affiliation—determines their voice in the discussion. I have witnessed many occasions when a question from a newly appointed practitioner proved more valuable than an answer from someone with 20 years of experience.

Over the past three years, more than 230 professionals from pharmaceutical and biotechnology companies, CROs, hospitals, universities, and regulatory authorities have participated, generating more than 3,500 questions. Topics have ranged from follow-up strategies for Ames-positive drug candidates and ADA-related changes in TK exposure to digital pathology, AI-based toxicity prediction, and genotoxicity assessment of mRNA vaccines. The range of subjects discussed provides a meaningful record of the challenges our industry has faced in recent years.

TRT is not a program operated by a particular institution. It is an open community built collectively by its participants. My role is simply to facilitate the process; the discussion always centers on the professionals who must make real-world decisions in the field. I will continue to support this community and help it grow.

We warmly welcome the participation of anyone interested.

Format
Participants regularly meet through an online video-conferencing platform to present and share their views on designated topics. In-person meetings may also be held.
In-person meetings are planned four times per year, and there are no membership or participation fees.
Company confidential information is strictly excluded, and discussions are limited to practical toxicology matters.
Eligibility
Anyone with at least one year of practical toxicology experience who is willing to participate actively in discussions is welcome to join.
Moderator
Professor Woo-Chan Son; participating members may subsequently take turns serving as moderator.
Discussion Topics
Topics related to toxicology and drug development
Membership Application