Rescue Studies - Imaging Endpoints

At Imaging Endpoints (IE), we understand that despite meticulous planning and execution, unforeseen challenges can arise during clinical trials. These challenges can disrupt the course of the trial, potentially impacting timelines, resources, and overall trial outcomes. That’s where our dedicated Rescue Studies Team comes in.

Our Rescue Studies Team is uniquely experienced in conducting rescue studies, providing swift and adept interventions to get your trial back on track. We leverage our industry-leading science, quality, and execution to ensure your trial recovers effectively and efficiently.

Why Choose IE for Your Rescue Study?

Remarkable Regulatory Approval Rate: With a 95% marketing authorization success rate globally, IE has a proven track record that leads the entire industry. And our perfect inspection record further underscores our commitment to quality and regulatory compliance. For any rescue study, we bring our thoughtful scientific and regulatory approaches together with focused resolve to achieve success where others may have failed.
Dedicated Rescue Study Team: Our team members are not just experienced; they are dedicated to conducting rescue studies. This focus allows us to provide the specialized attention and expertise that rescue studies require.
Advanced Data Analytics: Our focus on oncology and our advanced data analytics capabilities, including tumor growth kinetics (eTGK), radiomics, and more, allow us to provide unique insights and solutions during the rescue process.
Global Leader in Oncology Trials: As the largest oncology-focused iCRO, our experience in over 500 oncology trials globally, interacting with regulatory agencies worldwide, equips us with the knowledge and skills to navigate complex regulatory landscapes and get your trial back on track.
Unparalleled Availability and Partnership: We believe in working closely with our clients, providing unparalleled availability and partnership. We become an extension of your team, ensuring seamless communication and collaboration throughout the rescue process.
Connecting Imaging to the Cure: As the only iCRO focused on Connecting Imaging to the Cure, we optimize the opportunity to demonstrate efficacy while adhering strictly to regulatory expectations, enhancing the advancement toward registration.

Our Rescue Study Process

Our Rescue Studies Team, comprised of the world’s leading medical, scientific, data management, regulatory, and operations experts conducts a thorough review of your current protocol and study situation to develop a customized plan to course correct, focusing on the quality and expertise your study demands. We review the core issue(s), conduct a root cause analysis, assess the management of vendors, and review all necessary data in assembling a corrective plan to ensure your goals are met.

Let’s Get Your Oncology Trial Back on Track

No company wants to find themselves in need of a rescue for their trial, but when challenges arise, you can trust Imaging Endpoints to provide the highest level of expertise, guidance, and support. With our dedicated Rescue Studies Team comprised of global experts, our industry-leading regulatory approval success rate, and our perfect inspection record, we’re ready to get your study back on track.