We are a leading consulting and solutions provider in the industry for eCTD regulatory affairs & operations, and we were the pioneers of eCTD submission in Japan.
Our expertise encompasses a broad range of eCTD-related services, including authoring consultation to submission management and publishing service.

Expertise in any kind of submission to:
・PMDA (Japan)
・EMA/EDQM (EU)
・FDA (USA)
・HC (Canada)
・TGA (Australia)
・Swissmedic (Switzerland)
・FDA Thai (Thailand)

eSA, Inc.

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eSA, Inc.

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