eSA, Inc.

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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)
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