Shunee Yee to Judge 2010 Stevie Awards for Women in Business

2010年10月12日

After winning last year’s award, CSOFT is back to help select this year’s winner

New York, New York (October 12, 2010) Shunee Yee, CEO and President of CSOFT International, Inc. , has been invited to join the Board of Distinguished Judges & Advisors at this year’s Stevie Awards for Women in Business. The board features many leading women entrepreneurs and luminaries in business, and Shunee’s invitation to join the board is in recognition of her success in building CSOFT into a leading provider of multilingual localization, testing, and software development services with Fortune 500 clients around the globe. Based on this achievement, Shunee won the prestigious award for Best Asian Entrepreneur at last year’s ceremony.

“After having won last year’s award for Women in Business, I am honored to serve on the Board of Judges at this year’s event,” said Ms. Yee, CEO and President of CSOFT International, Inc. “Women engaging in business face huge challenges on so many levels, and it’s not only important but necessary that we acknowledge each other’s accomplishments—both to keep our chins up and make sure that the ball keeps rolling.”

The Stevie Awards for Women in Business feature over 50 categories including Executive of the Year, Entrepreneur of the Year, Young Entrepreneur of the Year, Company of the Year, Employer of the Year, Mentor of the Year, Female Employee of the Year, Women’s Blog or Web Site of the Year, and Marketing Campaign for Women of the Year, among others. The awards are produced by the creators of the prestigious American Business Awards.

All female entrepreneurs, executives, and the organizations they run worldwide, are eligible for nomination. The winners will be announced at an awards dinner in the Marriott Marquis Hotel in New York on November 12.

About CSOFT Health Sciences

CSOFT Health Sciences, leaders in clinical trial localization, provides AI/ML-enabled medical translation services for all phases of the drug and medical device product lifecycle, from development to post-launch. We also specialize in DCT solutions, linguistic validation, and CTD/eCTD submissions with the FDA, EMA, and NMPA. Our operations are certified in ISO 17100:2015, ISO 9001:2015, and ISO 13485:2016, ensuring our customized solutions meet the rigorous regulatory requirements of MMA, NDA, CTA, and Medical Device Application submissions. www.csoftintl.com

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