Research and Development

For many years since the start of our firm in 1981, we have been providing legal services to domestic and overseas pharmaceutical companies, medical device manufactures, bio-venture companies, research institutes, contract research organizations (CROs) and various other clients. Our services include advising such clients on license agreements (patents, trademarks, etc.), research and development agreements, clinical research agreements and material transfer agreements.
Recently, the lawyers who have expert knowledge and experience provide legal advice on cutting-edge areas such as iPS cells, antibody drugs, regenerative medicine, gene therapy, biotechnology and telemedicine from the view of intellectual property law, personal information protection law and other laws specific to such areas. In addition, we have a contracted advisor who is a former government official of the Ministry of Health, Labour and Welfare (MHLW) and the Pharmaceuticals and Medical Devices Agency (PMDA), which enables us to provide more practical and quality legal advice.

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PublicationsArchives

2026.01.30
Legal Affairs for Chinese Life Sciences and Healthcare No. 27: A Cross-border Staged Manufacturing Model for Pharmaceuticals
2025.11.28
Legal Affairs for Chinese Life Sciences and Healthcare No. 26: Progress in Domestic Manufacturing Policies for Medical Devices
2025.09.25
Legal Affairs for Chinese Life Sciences and Healthcare No. 25: Update on the Amendments to China's Medical Device Laws and Regulations
2025.05.27
Legal Affairs for Chinese Life Sciences and Healthcare No. 24: Update on the Revisions to Chinese Pharmaceutical Regulations
2025.03.24
Legal Affairs for Chinese Life Sciences and Healthcare No. 23: Updates on the Amendments of Pharmaceutical Laws and Regulations of China
2023.08.24
Thematic-based: Legal Practice in the Healthcare Business
2022.07.04
China's Life Sciences and Healthcare-No.2 -The Good Vigilance Practice rule in China
2022.03.14
A Legal Review of China's Life Sciences and 2 Healthcare- No.1 -General Introduction and MAH System
2022.02.21
Legal Affairs for Chinese Life Sciences and Healthcare (Part 7) - Amendment to the Cosmetic Supervision and Administration Regulation for the First Time in 30 Years, and the Subsidiary Regulations on Administrative Measures for Cosmetic Registration, the
2022.01.21
Legal Affairs for Chinese Life Sciences and Healthcare (Part 5) - Amendment to the Cosmetic Supervision and Administration Regulation for the First Time in 30 Years, and the Subsidiary Regulations on Administrative Measures for Cosmetic Registration, the
2021.11.24
Legal Affairs for Chinese Life Sciences and Healthcare (Part 4) - Developments in Amendment of Regulations Concerning Wholesaling/Retailing of Pharmaceutical Products, Etc. (Measures on Supervision and Control of the Drug Business and Usage Quality (Draft
2021.10.28
Legal Affairs for Chinese Life Sciences and Healthcare (Part 3) -Approaching the implementation of China GVP (Good Pharmacovigilance Practice) (effective from December 1, 2021) (2)
2021.09.30
Legal Affairs for Chinese Life Sciences and Healthcare (Part 2) -Approaching the implementation of China GVP (Good Pharmacovigilance Practice) (effective from December 1, 2021) (1)
2021.08.30
Legal Affairs for Chinese Life Sciences and Healthcare

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SeminarsArchives

2026.10.23
【Hybrid Seminar】】Series of Seminars on Life Science Practices (5): Designing Contractual Terms for Medical Device M&A--Closing Conditions, Consideration Adjustments and Duty of Cooperation
2026.09.30
【Online Seminar】Series of Seminars on Life Science Practices (4): Determination on Qualification of Software (App) as a Medical Device
2026.05.21
【Hybrid Seminar】Series of Seminars on Life Science Practices (1): Difficult Aspects of Pharmaceutical License Agreements
2024.07.11
【Online Seminar】 Series of Seminars on M&A in Various Business Fields (1): Pharmaceutical Industry
2022.10.04
【Onilne Seminar】Life Science Practice Seminar No.8: Legal Practices for Settlement of Pharmaceutical Patent Disputes
2022.04.26
【Onilne Seminar】Life Science Practice Seminar No.6: Learnings from Court Decisions on Defects in Pharmaceuticals, Medical Devices, Cosmetics, etc.
2022.02.09
【Onilne Seminar】Life Science Practice Seminar No.5: Practices of Compliance with the Pharmaceutical and Medical Device Act (Focusing on Development of the Compliance Structure and Monetary Penalty System)
2021.12.16
【Onilne Seminar】Life Science Practice Seminar No.4: Basic Points to Note in License Agreements for Life Science
2021.10.05
【Onilne Seminar】Life Science Practice Seminar No.3: Points to Note Regarding Joint R&D Agreements in the Field of Life Sciences
2021.05.27
【Online Seminar】Points to Note in Contracting with Overseas Bio Ventures
2021.04.16
【Onilne Seminar】Life Science Practice Seminar No.1: System Operation and Trends Regarding Regenerative Medicine Products as Observed in Recent PMDA Consultation/Approval Cases

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