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FACULTY

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細木 るみこ 細木 るみこ
Rumiko Hosoki
Professor
Rumiko Hosoki
Department
Department of Pharmacy
Laboratory
Regulatory Science Laboratory
Field of Study
Medical Pharmacy

History

Graduate School/University, etc.

1983 Graduated from Faculty of Pharmaceutical Sciences, Toho University 1985 Completed Second Term Doctoral Course in Medical Pharmacy, Graduate School of Pharmaceutical Sciences, Toho University 1995 Ph.D. (Pharmaceutical Sciences)

研究者になったきっかけ

Why I Became a Researcher

Before joining the (Independent Administrative Institution) Pharmaceuticals and Medical Devices Agency (PMDA), I was conducting pharmacology research. During my master's course, I was given a research theme related to Ca2+ in substance P in the iris sphincter. I was delighted after being introduced to the literature led to the development of my research on receptor subtypes, and I think that this was what got me started on my research. In addition, it seems like it was my time to learn the basics of building logic that were unknown to me up until that point. After that, I was glad to know that I had the same idea and was doing the same experiments at the same time as famous researchers overseas, and when this happened, my teacher said, "You should regret having the same idea as another researcher, even if they’re famous. What he said was eye opening to me. Immediately after joining PMDA (former Center for Product Evaluation), I was conducting quasi-drug approval evaluations. I started regulatory science research because I wanted to put out into the world a way of thinking about evaluations and the judgment of evaluations easier to understand.

Research Information

Research Area and Theme

A research study on the evaluation of effectiveness and safety of pharmaceutical products from both nonclinical and clinical trials.

I will investigate and analyze the evaluation of effectiveness and side effects of pharmaceutical products, including a perspective from the mechanism of action, using assessment reports and databases, etc., and seek out appropriate indicators of effectiveness and ideal safety measures. I also want to try to evaluate the effectiveness of quasi-drugs.

Thoughts on Research Theme

I would like to conduct a research study to determine whether there is any safety information that can be predicted from non-clinical data or the mechanism of action of a drug during the assessment process using an assessment report or database, and whether there are objective indicators of effectiveness to contribute to society so that it would be possible to provide effective and safe pharmaceutical products to medical sites in as soon as one day.

Message to Students

細木 るみこ 学生へのメッセージ 細木 るみこ 学生へのメッセージ

Message to Students

The first thing I felt when I joined PMDA was that "the Pharmaceuticals and Medical Devices Act (then known as the Pharmaceutical Affairs Law) is alive and breathing here!" In my classes, I would like to focus on making you truly understand the fact that the law is a living thing. If you look at the Pharmaceutical Affairs Law, it will be clear that the scope for graduates of the College of Pharmaceutical Sciences is wide. For myself, the various jobs that I’ve experienced as well as the friends and acquaintances that I’ve made have sustained me. So, to all of the students out there, I also ask that you make lifelong friends here.

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