ECOA CRO PARTNERSHIPS
Differentiate your next study proposal with IQVIA eCOA
Leverage the best-in-class eCOA platform and industry leading expertise from IQVIA Technologies to augment your study proposals and increase your win rate.
Leverage the best-in-class eCOA platform and industry leading expertise from IQVIA Technologies to augment your study proposals and increase your win rate.
Determine the optimal eCOA plan with subject matter experts.
Strategize on how the eCOA technology can optimize the capture outcomes related study objectives.
Identify license, translation and design requirements early to meet study timelines.
5-day turnaround after confirmation of the specific assessment.
Provide a comprehensive proposal (PowerPoint or Word) language.
Pricing to the study specifications.
Respond to any scope changes or price reductions required to win the business.
Support for BDM preparation with collateral and talking points.
BDM presence during meeting, as needed.
Product demonstration tailored to the use case.
We deliver a prescriptive outline of the services and design needed to optimize the trial execution.
We determine the optimal devices to use including Bring Your Own Device (BYOD) potential for the research study.
We provide comprehensive training for the investigative site and the Sponsor/CRO monitoring teams.
We have an instrument library and developer agreements to accelerate licensing and translations.
IQVIA offers a SaaS delivery model of our eCOA platform through a web browser and mobile app licensed on a subscription basis.
We have the right partnership option for you, whether the right technology to plug into your clinical development strategy or enhanced by IQVIA Technologies expertise and services.
This cloud-based solution collects participant outcomes with efficiency, agility, and transparency.
All the Technology Partnership program features plus the following.
Clinical trials face increasing pressure to deliver new treatments to market faster. IQVIA Connected Devices accelerates trial outcomes with medical device recommendations that fit your clinical study, deliver cleaner data, and speed data collection and analysis with lower patient and site burdens.
Power your decentralized trial with an agile randomization and trial supply management solution that supports supply flexibility and optimization as well as adaptable direct to patient options.
Deliver eConsent to sites and study participants around the globe with confidence