Ryoichi Nagata, M.D., Ph.D., FFPM

Board Director, President and CEO

Ryoichi Nagata, M.D., Ph.D., FFPM

Board Director, President and CEO

Ryoichi Nagata, M.D., Ph.D., FFPM is the Chairman and President of Shin Nippon Biomedical Laboratories, Ltd., Chairman of Medipolis Proton Therapy and Research Center, Chairman of Veritas Academy, and Honorary Consul-General of the Royal Government of Bhutan in Japan. He obtained MD from School of Medicine at St. Marianna University, PhD from Graduate School of Medicine at Kagoshima University, and MA from Graduate School of Buddhism at Koyasan University. He also serves as a member of board of directors for St. Marianna Univ., Juntendo Univ., The Japan China Medical Association, and Japanese Society of Preventive Medicine. Visiting Professor of St. Marianna University, Tokyo Medical University, Kochi University, Yantai University (China), and University of Maryland, Baltimore. He is qualified to be an Instructor for Clinical Pharmacologists of The Japanese Society of Clinical Pharmacology and Therapeutics, Instructor for Japanese Society of Preventive Medicine, Certified Toxicologist of The Japanese Society of Toxicology, and Fellow of the Faculty of Pharmaceutical Medicine of the Royal Colleges of Physicians (FFPM, UK).

Shunji Haruta, Ph.D.

Board Director and COO

Shunji Haruta, Ph.D.

Board Director and COO

Shunji Haruta, Ph.D., was appointed TR Company Vice President in April 2019, and he has been a Corporate Officer and a General Manager of the Company since January 2011. Dr. Haruta also currently serves as a member of the Board of Directors of SNLD Co., Ltd., a subsidiary of Shin Nippon Biomedical Laboratories. Dr. Haruta joined Shin Nippon Biomedical Laboratories Ltd. in April 2001, to develop the proprietary nasal drug delivery technology which was the first project in SNBL’s translation research business.  Dr. Haruta has contributed as an inventor creating numerous patents related to nasal drug delivery technology. New business based on the nasal drug delivery technology has steadily progressed by his dedicated efforts for over 20 years and as a result four instances of technology out-licensing have been achieved, so far. Prior to joining Shin Nippon Biomedical Laboratories Ltd., Dr. Haruta accumulated clinical experience as a clinical pharmacist at Miyazaki Medical College. Dr. Haruta received his Ph.D. degree from the Faculty of Pharmaceuticals Sciences at Okayama University.

Robert-Schultz

Robert Schultz

Senior Vice President and Head of Chemistry, Manufacturing, and Controls
Robert-Schultz

Robert Schultz

Senior Vice President and Head of Chemistry, Manufacturing, and Controls

Rob joined Satsuma in 2017 and currently serves as our Senior Vice President and Head of Chemistry, Manufacturing, and Controls (CMC). He has over 32 years of drug development experience, focused primarily on the CMC development of orally inhaled products, including VENTOLIN® inhaler and ADVAIR® metered dose inhaler (MDI) products. Rob began his career developing MDIs at Muro Pharmaceuticals (acquired by ASTA Medica). He then joined GlaxoSmithKline, followed by KOS Pharmaceuticals (acquired by Abbott). In these companies, he led CMC development initiatives for multiple inhalation products, including ADVAIR®, Serevent®, Flovent®, Ventolin®, Azmacort® and an insulin MDI product, while advancing into roles of increasing responsibility. Prior to joining Satsuma Pharmaceuticals, Rob was an early member of the senior leadership team at Pearl Therapeutics (acquired by AstraZeneca), where he led CMC and global project teams developing Pearl’s MDI products, including Bevespi Aerosphere® and Pearl’s triple combination product Breztri®. Rob received a B.S. degree in Biochemistry from Dartmouth College.

Mic-Iwashima

Mic Iwashima

Vice President & Head of Operations
Mic-Iwashima

Mic Iwashima

Vice President & Head of Operations

Mic was intimately involved in founding and spinning out Satsuma from Shin Nippon Biomedical Laboratories, and he has served as Vice President & Head of Operations since then. Mic has more than 15 years of experience in the field of nasal drug delivery and was involved in developing the technologies incorporated in Satsuma’s lead product candidate, STS101, as well as in preclinical development, early clinical evaluation and CMC development of multiple nasal-route, drug-device combination product candidates. Prior to joining Satsuma, Mic served in a variety of management roles at Shin Nippon Biomedical Laboratories, encompassing operations, product development, quality, regulatory affairs, business development and intellectual property management. Mic received a B.S.E. degree in engineering from North Carolina State University, where he also did research in the area of computational fluid dynamics of nasal airflow.

Shannon-Strom

Shannon Strom, PhD, R.A.C.

Vice President & Head of Regulatory Affairs
Shannon-Strom

Shannon Strom, PhD, R.A.C.

Vice President & Head of Regulatory Affairs

Shannon has served as our Vice President of Regulatory Affairs and Quality since 2018. Shannon has over 20 years of research and drug development experience with over 15 years as a leader in regulatory affairs. Shannon began her career through a drug development fellowship with Cato Research, a specialty contract research organization, and then transitioned into medical writing and regulatory affairs specializing in neurology and oncology product development from nonclinical studies through marketing approval. In 2010, Shannon moved to Pearl Therapeutics to focus on inhaled respiratory drug products, drug-device combination products, and product development through the US 505(b)(2) approval pathway. In addition to her regulatory leadership at Pearl, Shannon provided key inputs to Pearl’s nonclinical and clinical programs. Pearl Therapeutics received the FierceBiotech 2011 Fierce 15 award and was acquired by AstraZeneca in 2013 for $1.15 billion. Shannon has led global regulatory strategy programs including regulatory health authority interactions and approval of multiple new drug applications, including most recently approvals of Bevespi Aerosphere® and Breztri®. Shannon received a B.S. in biology from Duke University and holds a PhD in pharmacology from the University of North Carolina at Chapel Hill.

David Prichard

Vice President of Manufacturing Operations

David Prichard

Vice President of Manufacturing Operations

Dave joined Satsuma in 2019 and currently serves as Vice President of Manufacturing Operations.  Dave has over 20 years of drug/device combination product manufacturing and packaging experience with roles in Engineering, Validation, Quality and Operations Management.  Dave began his career with Procter & Gamble, followed by GlaxoSmithKline and Pearl Therapeutics (acquired by AstraZeneca).  Dave received a Bachelor of Mechanical Engineering degree from Georgia Tech, and an M.B.A. in Finance from the University of Cincinnati’s Lindner College of Business.