Meet with Christopher Kata and the TrialStat team during the Clinical Outsourcing Group CRO Summit, December 3rd – 4th in Raleigh, NC!

Your eClinical Technology Should Adapt To Your Protocol

You should not have to compromise your study design simply because your eClinical Technology does not support your unique study requirements.

At TrialStat we do things differently. We believe that you should not have to compromise and to make that a reality, we specialize in Custom Validated Development. Whether it's a small change in workflow, a special randomization methodology, integration with a medical device, or development of an entire custom module. We have the experience and regulatory expertise to make this happen.

In many cases, we also cover the development costs and ensure it is ready for your study.

With full service, flexible, and cost-effective Study Development services across all phases of clinical research, as well as custom technology implementations, integrations and custom features.

TrialStat is your trusted partner in custom development and integration projects.

• Experienced developers provide collaborative support on your specific technology needs
• Compliant with all regulatory requirements such as 21 CFR Part 11, HIPAA, GDPR, and including Master Validation Packages / Plans
• Detailed knowledge of technology advancements and system integration requirements ensures no wasted time or effort at scoping or during execution, reducing overall project costs

If you have unique study requirements and are in need of a partner that is willing and able to work with you, then call us today and schedule an exploratory meeting with our solution experts.