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Generate Regulatory-Grade Data

Accelerated pipeline research and development leading to FDA approval for drug submissions

Broad experience managing and curating data from more than one million patient records, and providing curation support for more than 500 clinical trials

Omega does not retain rights to, or copies of, any data we are trusted to curate.

Accelerated pipeline research and development leading to FDA approval for drug submissions

• Comprehensive data for FDA submission
• Actionable data leading to improved decision making
• Timeliness for quick action on research findings
• Auditability for accountability from data results
• Governance to ensure standards are met
• Standardization for consistent results

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