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eCTD Submit

Ownership: Private
Development stage: Other

Overview

ECTD Pharma specializes in regulatory document preparation and electronic Common Technical Document (eCTD) submissions for pharmaceutical, biotech, medical device, and life science companies. They have managed over 5,000 submissions with a 100% acceptance rate by health authorities such as the FDA and EMA. Their expertise covers INDs, NDAs, clinical trial applications, and ongoing lifecycle management of regulatory dossiers using proprietary software solutions.

Industry: Contract Research Organization

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