Ensure HIPAA-compliant document sharing for clinical trials, regulatory submissions, and M&A transactions. Secure collaboration for pharmaceutical companies and healthcare providers.
Full HIPAA compliance with Business Associate Agreements (BAAs), ensuring protected health information (PHI) is handled according to federal regulations.
Military-grade 256-bit AES encryption for data at rest and in transit, with secure access controls and audit trails for all document interactions.
Streamline FDA submissions, clinical trial documentation, and regulatory filings with organized document management and version control.
Enable secure collaboration between pharmaceutical companies, CROs, healthcare providers, and regulatory bodies with granular permission controls.
Manage clinical trial documentation, patient data, protocol amendments, and site communications securely. Share trial results with regulatory bodies and stakeholders while maintaining HIPAA compliance.
Facilitate healthcare M&A due diligence with secure sharing of patient records, financial data, regulatory compliance documents, and operational metrics. Maintain confidentiality throughout the transaction process.
Organize and submit FDA applications, drug approval documentation, medical device certifications, and post-market surveillance reports. Track submission status and manage regulatory correspondence.
Enable secure collaboration between research institutions, pharmaceutical companies, and academic partners. Share research data, lab results, and intellectual property documentation safely.
Reduce compliance risk with automated HIPAA controls
Accelerate regulatory approval timelines
Improve collaboration between stakeholders
Maintain comprehensive audit trails for all access
Protect sensitive patient and research data
Streamline document organization and retrieval