InoRx - Your Home for Rescue Studies

Why Sponsors Call InoRx

Right Patients

Right Time

Right Outcome

When a study stalls, sponsors need urgent, objective, and accountable answers. InoRx brings senior therapeutic-area, regulatory, and operational leadership to diagnose root causes and execute rapid study recovery without unnecessary delays.

Proven from Diagnosis to Recovery

Stabilize in days

Sponsors don’t lose another quarter

A fix that holds up

to the regulator

One team owns the outcome

from start to finish

Why Sponsors Call InoRx First

Urgency with accountability — backed by proof and white-glove execution.

Independent Rescue Diagnostic

We start with the truth, not a pitch

The InoRx Rescue Score provides an objective, fixed-scope assessment across seven critical domains—giving sponsors a clear view of what is failing, why it is failing, and what can realistically be recovered before making the decision to change CROs.

Rapid Activation & Hospital-Site Network

Stabilize in days – sponsors don't lose another quarter

InoRx combines rapid operational activation with an established hospital and site network, allowing sponsors to address enrollment and execution gaps without waiting on another provider to build the infrastructure needed to recover the study.

Regulatory & Root-Cause Excellence

Fix the cause—not just the symptoms

Senior therapeutic-area and regulatory experts identify the underlying drivers of study failure and build corrective actions that address the root cause—designed to restore performance while standing up to regulatory scrutiny.

Dedicated Ownership & Governance

One accountable team owns the outcome from start to finish

A dedicated senior InoRx lead remains engaged throughout the rescue, coordinating priorities, driving corrective actions, and maintaining governance until the study is back on track. We intervene where the study is broken—without forcing an unnecessary full CRO replacement.

66+

Studies

4,900+

Subjects

11

Therapeutic Areas 

Phase I–IV

Clinical Execution 

+15

Years of SRM-CCTR clinical excellence

What Services We Offer?

InoRx Rescue Studies Span the Full Arc

Diagnose

Deliverable: Diagnostic report + Go/No-Go readiness

Decide

Deliverable: Go/No-Go decision + recovery plan

Mobilize

Team assignment — Rescue PM + functional leads appointed
Contracting — Sponsor / site / vendor contracts initiated in parallel
Study transition — Critical documents, systems, data & handover initiated
Execution setup — Sites, vendors, systems & resources aligned for execution
Rescue launch — Recovery plan activated, execution begins

Deliverable: Rescue / recovery plan initiated to meet revised milestones

Deliver

Study recovery — Close critical gaps across sites, enrolment, data, monitoring & backlog
Re-baseline & control — Critical path, milestones, schedule & forecast
Drive performance — Site, enrolment, vendor & functional performance
Resolve & correct — Risks, issues, dependencies & corrective actions
Govern & stabilize — Integrated governance, escalation, change control & delivery predictability

Deliverable: Study back on track, in motion

Ongoing Control & Governance

Continuous oversight to keep recovery on track.

Control runs across every stage

Continuous oversight, clear visibility, and rapid action keep every stage of recovery on track.

Real-time tracking & milestone reporting

Track study progress against critical milestones and recovery targets.

Sponsor governance cadence

Maintain regular governance and transparent communication with the sponsor.

Continuous quality oversight

Monitor quality, risks, issues, and corrective actions throughout execution.

Escalation management

Identify and escalate critical issues quickly to protect timelines and delivery.

Proven Study Rescue in Action

Explore how InoRx helps sponsors diagnose stalled studies, address root causes, and restore clinical execution—bringing studies back on track with speed, accountability, and regulatory confidence.

Stabilizing a Distressed Medical Device Rescue Study

Experienced project management intervention resolved site-level operational, compliance, data, training, and vendor issues, helping return a 2,000-participant medical device study to on-track execution

Meeting a Late Regulatory Mandate Rescue Study

Rapid Phase I site activation, participant pre-screening, and coordinated execution helped a sponsor meet a late regulatory mandate within a highly compressed timeline

Delayed Startup to Success Rescue Study

Rapid site activation and flexible enrollment capacity helped recover a delayed study, absorb additional participants, and complete study activities before the reference clinical trial material expired

Rapid Assessment. Decisive Action. Dedicated Ownership.

When your study stalls, bring it back on track with InoRx.