Part of the Clinical Cadence Ecosystem

Eliminate Regulatory Bottlenecks.
Activate Sites in Days.

TurboRegsTM turns every regulatory packet into a 1-click workflow —
extracting data, filling forms, validating completeness, and orchestrating routing instantly.

Transform Your Regulatory Workflow

See how TurboRegsTM revolutionizes site activation compared to traditional methods

The Old Way

  • CVs and Medical Licenses scattered
  • Chasing missing signatures
  • High-touch QC cycles
  • 30–90 days lost due to rework

Your ROI

  • 50–70% faster regulatory packet generation
  • Zero missing fields
  • Hundreds of coordinator hours saved
  • Faster IRB submission → faster activation

From Scattered Documents To
Complete, Validated Packets - Instantly

Chaos in Clarity out

CV
Medical
License
Financial
Disclosure
1572
Certification

Scattered & Disorganized

TurboRegsTM

Processing...

Complete Packet
Ready for submission
All fields complete
All signatures captured
No expired documents
Institution templates applied

Complete & Validated

Trusted by Sponsors, AMCs, and CROs
Accelerating Activation

Join the leading research organizations transforming their regulatory workflows

"What used to take days now takes minutes."

CRC
Clinical Research Coordinator

Academic Medical Center

"We no longer chase signatures or missing docs."

RAM
Regulatory Affairs Manager

Multi-Site CRO

Why TurboRegsTM?

The strategic framework behind our regulatory automation engine

01

The Visceral Problem

Regulatory packets stall activation because forms, CVs, certifications, licenses, and site documents live in scattered systems — or worse, in local folders that no one can see.

02

The Differentiated Solution

TurboRegsTM automates packet creation, fills forms instantly, and eliminates rework so startup teams never start from zero.

03

The Defendable Outcome

Organizations activate sites faster, reduce errors to zero, and finally operate without manual firefighting.

Ready to transform your workflow?

Create Your Free Account

Join trial activation teams that are eliminating regulatory bottlenecks and
activating trials in days, not months.