ClinicalTrials.gov Publishing

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Pharmapace provides end-to-end support for ClinicalTrials.gov publishing, ensuring full compliance with federal registration and results reporting requirements. Our team handles the accurate and timely submission of study records, helping sponsors meet regulatory obligations, enhance trial transparency, and maintain public trust. With deep knowledge of NIH and FDA guidelines, we streamline the entire process so you can stay focused on your clinical development goals.

Our services include:

• Initial trial registration and updates
• Results posting in compliance with FDAAA and NIH policies
• Data formatting and QC checks
• Ongoing maintenance and submission tracking
• Liaison support for communications with ClinicalTrials.gov