IMPROVE IMAGING QUALITY AND RELIABILITY
Imaging in clinical trials has seen tremendous growth as evidenced by the number of trials initiated over the past two decades. Additionally, imaging data is increasingly used as the primary endpoint for some related trials. Put our expertise in drug, device and biologic imaging to work for you.
MINIMIZE MANUAL ERRORS AND BIAS, MAXIMIZE VISIBILITY
Improve data quality and run more efficient studies with integrated software and systems specifically built for clinical trials. Benefit from our advanced technology combined with deep scientific and regulatory expertise in key therapeutic areas to get seamless and secure collection, evaluation, management and reporting of high-quality, objective imaging endpoint data.
GREATER DATA CONSISTENCY
Clinical trials require quantitative, reproducible processes to deliver consistent data. Reduce errors by up to 20% via advanced automation that ensures adherence to scoring criteria and eliminates manual activities prone to mistakes.
CONTINUOUS DATA TRANSPARENCY
Experience 100% visibility into your data at any time, from upload to data transfer. Get within-visit enrollment evaluations and enable a comprehensive and compliant audit trail with our singular, purpose-built platform.
GREATER DATA OBJECTIVITY
Reduce reader bias and discordance through consistent measurement tools with automated scoring criteria and calculations. This proven, high-tech approach enables experts to focus their efforts on the areas of greatest impact.
PUT SMARTER, FASTER IMAGING TO WORK IN YOUR TRIAL
Manual, outdated imaging based on paper case report forms (CRFs) and one-size-fits-all workflows cause compliance and data quality issues throughout a clinical trial. Reduce cost, time, subjectivity and data variability with integrated technology, processes and expertise that’s adapted to your specific study protocol.
Facilitate timely eligibility and enrollment decisions while ensuring scientific validity and yielding higher-quality data with our purpose-built imaging technology. Sites will be compliant – and more productive – via automated image upload, quality assurance, and removal of Protected Health Information (PHI) from your imaging data.
Ensure a strong connection between your image data inputs, observations, measurements and scientific outputs, scores and endpoints by automating data management processes. Even better, your trial will be compliant with global regulators through a comprehensive audit trail that provides complete transparency and visibility into your protocol-specific workflows.
DIVERSE IMAGING EXPERIENCE
Get confidence in your trial results by working with our team of imaging and regulatory experts, who have diverse experience that spans protocol management and widely-used disease response criteria. We’ll partner with you to develop and review your protocols while managing your daily trial operations.
TAKE A CLOSER LOOK
Three Questions: Trends in Clinical Trial Imaging
Read insights from ERT’s Tim Kulbago about trends driving the increased use of imaging in clinical trials and how you can benefit from the use of advanced, technology-based imaging in your development programs.
ARTICLE: IMAGING INNOVATIONS
Learn how a combination of advanced technology and effective site radiologist training enables sponsors to reduce error rates and ensure the highest quality data when imaging endpoints are used in oncology clinical trials.
INFOGRAPHIC: IMAGING IN CLINICAL TRIALS
Poor-quality imaging data compromises decisions and, ultimately, regulatory decisions. Learn how technology-based solutions minimize risk and instill confidence in clinical trial imaging.
eBOOK: OVERCOMING IMAGING CHALLENGES
Get practical guidance on how to successfully generate accurate, quantitative imaging data that minimizes uncertainties and risks.
REQUEST A DEMO
Experience the future of imaging today. Submit your contact information and we’ll be in touch to schedule a demo.