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医薬品の開発に
「実りある」
​患者・市民参画を育てる

Multi-stakeholder Co-creation
Social co-creation with patients and public

Inclusive and sustainable participation from diverse backgrounds

Equitable and reciprocal benefits

Ongoing opportunities for mutual learning – not just receiving support or making requests

Concrete actions

Robust planning to return value to society

Clinical Trial Ambassador Project

Empirical research 'Using PED as Evidence'

A pilot case study 'Building PED using metaverse'

Patient-focused clinical trial ecosystem

Supporting citizen science

Interdisciplinary Approach to Science

Empirical research activities that foster patient and public involvement (PPI)

A Focus on Societal Implementation

Consultation to implement PPI

We offer consultations on PPI
in medicines development and clinical research.
Our team—representing various professional backgrounds—works with
companies, researchers, healthcare providers, and patient groups
to help put PPI into practice.

Participation in PFMD's initiative

Patient engagement and patient experience data

Patient engagement in health technology assessment

Global clinical trials ecosystem

Co-hosted by 1st PEOF+ Asia Pacific in Manila in 2026.

A Global Perspective

Systematizing PPI through international collaboration

News

2026.4.7

We have compiled a list of publicly accessible resources for learning about medicines development. Each resource is accompanied by information on its intended audience. This list was created as one of the outputs of the 2025 internship program.

  • List of Resources for Learning about Medicines Development (Japanese) ➡️

2026.4.7

We have compiled a list of publicly accessible resources for learning about medicines development. Each resource is accompanied by information on its intended audience. This list was created as one of the outputs of the 2025 internship program.

  • List of Resources for Learning about Medicines Development (Japanese) ➡️

2026.4.7

We have compiled a list of publicly accessible resources for learning about medicines development. Each resource is accompanied by information on its intended audience. This list was created as one of the outputs of the 2025 internship program.

  • List of Resources for Learning about Medicines Development (Japanese) ➡️

2026.3.31
 

The Ministry of Health, Labour and Welfare has issued "Regarding the Handling of Information Provision Related to Clinical Trials" (dated March 30, 2026, Pharmaceutical and Medical Affairs Bureau Notification No. 0330-1) and two related notices (➡️: Access to Ministry of Health, Labour and Welfare documents).

  • Regarding the handling of information provision related to clinical trials, etc. ➡️

  • Q&A regarding the handling of information provision related to clinical trials, etc. ➡️

  • Q&A regarding information provision by patient groups, etc., concerning clinical trials, etc. ➡️

2026.2.20

The proceedings of the 1st Roundtable on Patient Engagement and Patient Experience Data (PED) in Japan (we organised on October 18, 2025) have been published in Clinical Evaluation, Vol. 53, No. 3 .

  • English (original) ➡️

  • Japanese translation➡️

Public consultation

Public comment collection on new systems and guidelines regarding patient and citizen participation
 
We are currently soliciting public comments on the following new laws and systems. Anyone can submit their opinion.

If you have any questions, please contact us here: nobutaka.yagi@yoriailab.com

Events & Projects
Highlights
New Resources ➡️

Meaningful Engagement
 

The discussion we presented at the Sequential Meetings - Consensus for Global Research Ethics and Meaningful Engagemen has been published in the December 2025 issue of Clinical Evaluation. YORIAILab endorses the Statement for Global REsearch Ethics Norm and Meaningful Engagement (GREEN Statement), which was adopted following a series of deliberations at the conference.

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Our Partners
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