Takahiro Haruyama

President, Globizz Corporation

Takahiro (Harry) Haruyama is the founder and President of Globizz Corporation. Globizz Corporation provides consulting services for various U.S. regulations including U.S. FDA specifically to non-US companies that wish to do business in the U.S. 

For several years Harry gained practical experience in the United States medical equipment market which led him to eventually start a medical device sales company for the US and European markets. Afterward, Harry moved on to work for a medical device company where he was responsible for the development of medical devices. Harry has been involved in various medical device developments, including the development of artificial joints in the orthopedic field and product development in the respiratory field. During this time, he also accumulated an extensive amount of experience in clinical and other settings in medical device development. 

In addition, Harry is one of the few people in the welfare and medical business with a thorough knowledge of both the Japanese and U.S. markets. This knowledge includes development in products, regulatory filings, insurance coverage, distributor issues, sales, and after-sales service. Harry also understands regulations and strategies for entering the U.S. market for welfare and medical equipment, building sales networks, local production, M&A, and applying for U.S. medical insurance coverage. 

His experience has created a unique multicultural business ability and background, which has led him to expand his vision to various countries including Japan, the United States, India, Korea, and Europe. Nearly 20 years of FDA and medical device consulting experience has led him to serve as an officer of a U.S. subsidiary of a medical equipment manufacturer while running his FDA consulting company, Globizz Corporation.

a testing engineer and auditor for nearly three years. In 2020, I joined SAASCO Ltd., where
my main responsibility as a consultant is preparing technical documentation in accordance
with the MDR (Medical Device Regulation).