industry leader in study startup

join leading sponsors, CROs and sites who start studies smarter

goBalto speeds clinical trials through site identification, feasibility, selection, activation and into conduct — getting needed therapies to patients sooner, like our namesake, Balto 

webinar:  Dismantling data silos to improve study startup and mitigate risk
chromoreport:  Industry's first study startup performance metrics report
goBalto select:  goBalto and Informa partner to accelerate site selection for global clinical  trials

industry-proven experience

over
30%
reductions in cycle times. driving efficiencies, entry to market and therapy availability
over
100,000
sites activated 70+ country-specific “smart” workflows
over
75%
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adoption by global top pharmas & CROs
improve
Operational Performance

Automate the manual, cumbersome and error prone processes and tools, not specifically built for study startup, for site selection, feasibility and activation in clinical trials.

Read Case Study

goBalto Activate offers enhanced visibility into the traditionally cumbersome process of activating sites for clinical trials. The system creates efficiencies through streamlined communication among sites, sponsors and CROs. This ultimately drives shorter timelines and cost savings for our customers.

drive
Oversight

Simplified with a single on-demand view, delivering instant status updates on study progress, irrespective of how many concurrent studies or vendors you work with.

Select simplifies the process of finding investigative sites by ensuring optimal fit and its integrated workflows allow our globally dispersed clinical research teams to collaborate in real-time. Investigative sites can then be quickly setup to enroll trial subjects using Activate.

ensure
Risk Identification & Mitigation

Reduce your clinical trial risk by deploying purpose-built study startup technologies that aid in risk management.

goBalto's end-to-end study startup solution stood out for the opportunity it provides us to eliminate traditional bottlenecks in the flow of clinical data, which can impact study quality and lead to unnecessary delays.

leverage
Business Intelligence

Discover bottlenecks and areas for process improvements with custom analytics and real-time metrics into on-going operations. Find out where to focus your efforts.

With the granular level of business intelligence provided by goBalto we are able to make timely interventions and course corrections, as well as uncover insights into processes ripe for future enhancements – ultimately leading to timeline reductions and enhanced operational performance.

deliver
Organizational Compliance

Automate activities & document workflows with country-specific "smart" workflows that deliver global regulatory and SOP compliance.

Activate's workflows standardize processes and guide our clinical operations teams to complete and track specific documents and tasks for any site, country, or study based on regulatory requirements and our company's standard operating procedures (SOPs).

awards

Pharma Tech Outlook Top 10 eClinical Trial Management Solution Providers 2018
2018 Clinical and Research Excellence Awards Finalist
goBalto Named Scrip Awards Finalist
goBalto Awarded Top 20 Most Promising Biotech Technology Solution Providers 2017
goBalto Named Clinical Research and Excellence Awards Finalist
goBalto Selected as a 2014 Red Herring Top 100 Global Company
goBalto Named Cloud Trailblazer in Annual Trailblazers Awards
PM360 Innovator 2015
goBalto Awarded Top 20 Most Promising Biotech Technology Solution Providers by CIOReview Magazine
goBalto Named Clinical Research and Excellence Awards Finalist
Gartner Names goBalto a 2015 'Cool Vendor in Life Sciences'
2014 Interaction Awards
Rock Health Honors “Top 50” Digital Health Entrepreneurs
Fierce's Top 10 Biotech Techies - 2013
2012 Partnerships In Clinical Trials Award
BioIT World Best Practices Program Award

press

Dismantling Silos by Embracing Business Intelligence
Distributed Ledgers Can Streamline Clinical Trials
Wide inconsistency observed among clinical trials’ startup time
Improving SSU and the Clinical Trial Continuum
Assessing Study Start-up Practices, Performance, and Perceptions Among Sponsors and Contract Research Organizations
Why Are Metrics Important in Starting Clinical Trials?
Top 25 Biotechnology Solutions Providers 2017
Are Site-Less Trials the Future of Clinical Research?
Are delays in clinical trials due to a lack of experienced CRAs
The perils of building clinical trials on a shaky foundation
Myopic focus on Dashboards may Blur Insights
How CROs Are Helping With Healthcare’s Data Problem
Are Local IRBs Really Necessary?
To improve drug development, it’s time to rethink clinical trial site engagement
First Mover Does Not Always a Market Leader Make
To you it’s a document; to me it’s my life
Barriers to Increased Participation of Minorities in Clinical Trials
Accelerating Innovation to Cut Drug Prices
10 Tips for Enabling Better CRO-Sponsor Collaborations
Concomitant medications in clinical trials: Why the stakes are high
It’s Site Selection, Not a Toss of the Dice
The Cloud: speeding drug delivery
goBalto: Optimizing Clinical Studies
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Utilization of the Crowd for Medical Research
Rethinking 'Patient Centricity'
Better Study Startup Means Less Study Rescue
The Need For Speed In Clinical Study Startup
Expediting Study Startup Across the Globe
Study Startup: New Battleground in CRO Differentiation Strategy
Speeding Study Startup Through Better Collaboration and Data Flow
Q&A: Mush, you huskies!
Clinical Trials and the Power of the Cloud
BI the Way
How Much Transparency is Too Much?
Three Questions
goBalto goes for speed by reducing manual processes in study startups
Bringing Transparency and Collaboration to CRO Oversight
Accelerating Clinical Trials