HIPAA & GDPR Ready

Life Sciences & Clinical Research (CRO)

Native automation for Microsoft Outlook. Secure distribution of trial protocols, ethics approvals, and investigator updates.

The Transformation

The
Value Engine

Discover why industry leaders are moving away from generic cloud relays to local-first automation.

The Challenge

Managing communication with hundreds of investigator sites while strictly adhering to HIPAA and GDPR standards.

Cloud-based relays often fail strict clinical data compliance audits.

Manual distribution of trial documentation is prone to version errors.

Managing PII requires local-only processing to ensure patient privacy.

The Advantage

Native automation built for security and scale.

Zero-Cloud Architecture

Trial data remains 100% within your secure infrastructure.

Localized Audit Trails

Generate immutable logs of every sent transmission.

Secure Mapping

Map unique site protocols to specific investigators.

Workflows

How You Can
Leverage FlowDrafts

Transform your outreach with these mission-critical workflows.

Protocol Distribution

Distribute latest trial protocols to all investigator sites.

Investigator Updates

Send urgent safety updates and trial status notifications.

Ethics Reporting

Coordinate ethics committee reporting with full audit trails.

Result Notifications

Automate distribution of trial results to research partners.

Insights

Related
Guides & Insights

Deep dives into how Life Sciences & Clinical Research (CRO) teams optimize their Outlook workflows.

Workflow Guide

Healthcare Admin: Project Updates

Secure project updates for Healthcare Admin teams.

Read Full Guide
Workflow Guide

Clinical Research: Project Updates

Secure project updates for Clinical Research teams.

Read Full Guide
Workflow Guide

Healthcare Admin: Compliance Notices

Secure compliance notices for Healthcare Admin teams.

Read Full Guide

Ready to secure your clinical trials?

Join leading CROs and research institutions who trust FlowDrafts for clinical outreach.