Why Choose EloquiMed for CTD Summaries?
- Deep expertise in global regulatory submissions
- Strategic, persuasive, and compliant documentation
- Collaborative approach with your regulatory teams
Common Technical Document (CTD) Summaries & Overviews
Expert preparation of CTD summaries and overviews for global regulatory submissions, ensuring clarity, compliance, and strategic positioning.
Module 2 Summaries
Preparation of high-impact Module 2 summaries (2.3, 2.4, 2.5, 2.6, 2.7) for NDAs, BLAs, and MAAs.
Strategic Overviews
Expertly crafted overviews that highlight your product's value, benefit-risk, and regulatory strategy.
Global Compliance
CTD documents aligned with FDA, EMA, PMDA, and global regulatory requirements.