🔍 Advertising Regulation in Japan (Promotional Material Review) and Artificial Intelligence JP/EN
Ethics · Regulation · Technology — Pharma Practice Notes

Somewhere, someone is trusting that medicine.

That trust is held up by the daily judgments of every person working in pharma.
A learning notebook that supports those judgments, in one place.

💬 Ask the AI chat (experimental) →
↓ Purpose · Mission · Vision · Values
Purposewhy we exist

To keep living up to trust.

Every task in pharma, in the end, comes down to one question: "Did we live up to the patient's trust?" A single act of bad faith can erase, in an instant, trust built up over many years. Trust is not something handed to you as a result. It is what each of us must protect, judgment by judgment, every single day. This site gathers the learning that supports those judgments.

Missionwhat we do

Sustain a culture of self-examination, without interruption.

The most important thing for preserving trust is the discipline of periodically questioning ourselves. We continuously publish current developments and historical lessons in a verified form, creating a "space for self-examination" that one can always return to. Only material that has passed verification is placed here, regardless of format or domain.

Visionfuture we aim for

A future where each person can explain their work's meaning in their own words.

Pharma is a profession that takes on others' lives. By right, it should be one of the most respected industries in society — but the memory of drug-induced harm, conflicts of interest, and dishonest promotion has made it difficult for individuals to speak proudly about their work's significance. We aim to recover, from the ground up, an industry where each person can explain in their own words why their work matters.

Valueswhat we hold dear

Hold up an attitude of continual questioning as the prerequisite of every material.

01 — Ethics
Ethics begins where rules end.

"Not violating the rules" and "being ethical" are different things. When in doubt, we anchor not to the letter of the rule but to "the patient in front of you, and the version of yourself ten years from now." Ethics is not the memorization of answers — it is the attitude of continuing to ask.

02 — Regulation
Regulation is the collective memory of an industry.

The laws, self-regulatory codes, and guidelines that exist today are agreements forged in exchange for past drug disasters and incidents. Memorizing the text is not enough — only by reading the stories behind them do regulations become internalized. Read them not as "annoying rules" but as the testaments of those who came before.

03 — Technology
Technology is a means.

Technology is merely a tool that gains meaning only when it reaches the patient. We prize asking well, choosing well, and stopping well over the pursuit of the latest. The starting point is "we use it because we should," not "we use it because we can."

Contents

All 5 Groups · 18 Chapters

Foundations of pharma / Regulation and field practice / Perspectives / AI series / Daily notes ── the full chapter map aligned with the top navigation.

💬 AI Chat Desk experimental

Answers your questions on the spot, grounded only in materials stored on this site. It uses Anthropic's Sonnet, which can be wrong, so please verify against primary sources yourself before relying on any answer. A consent check appears on first use.

Open chat →
Foundations of Pharma
Regulation and Field Practice
01

Drug Disaster History

From sulfanilamide to the opioid crisis. The classic cases that built regulation, Japan's drug disasters, and modern scandals ── 10 chapters.

View chapter →
02

Ethics

What ethics is. Nuremberg to Helsinki, the four principles of medical ethics, corporate and individual professional ethics ── 8 chapters.

View chapter →
03

Compliance

Conflict of interest, anti-bribery, internal control, data integrity, whistleblowing — both personal conduct and organizational design ── 6 chapters.

View chapter →
04

Advertising Regulation

PAA Articles 66-68 / Advertising Appropriateness Standards / MSA Guidelines and their Q&A / JPMA Code / the JPMA material-creation guide ── 7 chapters.

View chapter →
05

Material Review

The map · international lens · mindset · solitude · risk · perspective · per-medium practice · culture ── 8-part / 29-volume series.

View chapter →
06

Production Quality Management

Quality assurance for client-commissioned materials. Regulatory conformance / AI review / QC·QA SOPs / four-signature delivery. NEW.

View chapter →
07

Material Requester (Manager)'s Responsibilities

The intermediate gate before vendor deliverables get forwarded into internal material review. A moral-responsibility framework. NEW.

View chapter →
08

Reviewer Development

Material review depends on people. Two series × 10 parts: an 8-dimension competency framework and a qualification bar for independent review. Material Review 2.0 for the AI era. NEW.

View chapter →
Perspectives — Studying the Self, Understanding Others
AI Series
Column
📋 Full sitemap  ·  🔍 Site search  ·  📅 What's New
About

About this site

Advertising Regulation in Japan (Promotional Material Review) and Artificial Intelligence is an individually-run educational portal for those facing ethics, regulation, and technology in the pharmaceutical industry. Materials are added continuously across domains.

Editorial Stance

An independent editor with hands-on experience in pharma, building this site as a place where ethics, regulation, drug-disaster history, and AI are connected through a single question: how do we keep living up to the patient's trust?

VisitorsJapanesePage views
VisitorsEnglishPage views
VisitorsTotalPage views
Visitors: same IP counted once per 30 days · Page views: total opens (PV)