More projects! Better Management! Without Intermediaries!
Stop missing out on opportunities and take your clinical trials to the next level. Medinexo connects you directly with Sponsors, eliminating barriers and maximizing your income.
The Sponsors are there, but how do you decide between thousands of investigation centers?
Without a network that supports you, you can easily be invisible to the big players in the industry.
Everything from documentation to audits, creates what seems to be a neverending workload.
The FDA, COFEPRIS, INVIMA, ANMAT… each entity has requirements that demand time and funds.
How many times have you sacrificed your budget to work with CROs that do not deliver optimal results?
The lack of communication between your team and the Sponsor delays projects and causes money loss.
Without continuous training, updated credentials, and efficient coordination, it is difficult to meet the Sponsor’s standards.
Once a project has finished, many sites tend to pause, waiting for new opportunities.
Medinexo helps you overcome these challenges with its exclusive Site Prime program, designed to transform your clinic, hospital, or site to attract Sponsors.
Medinexo actively promotes your center to Sponsors in our global network, increasing the probability that you will be chosen for high-level projects.
Sponsors around the world trust in the Prime Sites verified by Medinexo to lead their most innovative and funded trials, giving you priority on projects that are not available for other sites.
We guarantee to meet international compliance standards such as HIPPA Compliance, Part 11 Compliance, and more required by the FDA, COFEPRIS, INVIMA, and other global regulatory entities.
Access to leading tools including CTMS, e-Consent, and telehealth that optimize your workflows and reduce your response time. Digitalizing and simplifying your administration!
Sponsor visibility of your matching patient populations for clinical trials.
Monetize the anonymous clinical data of your patients while respecting all of the international regulations of data protection.
We provide e-learning, offering certifications and accreditation so your team is always prepared and competitive at the international level.
ResearchNexo Readiness methodology ensures that your site is ready to receive new trials.
With PRIME SITE, you not only optimize your operations and generate additional income, but you also position your site as a point of reference in global clinical research.
Every day that goes by without taking action is a lost opportunity to grow your research site. Medinexo is the key to opening doors to financed projects and securing a space as a prominent, global research center.
Compare the options and discover how the PRIME SITE subscription will transform the way your site operates.
With Prime, you will have visibility, advanced certifications, additional income, and access to Sponsors around the world.
With SITE PRIME + CTMS, you will have a Clinical Trail Management System that you can use for any trials brought to you directly by Sponsors, CRO or though the Medinexo network.
The CTMS provides a warehouse of data that can be applied consistently across data views within a study, and applied consistently across studies. The CTMS also provides controlled user accounts, so that data is accessed by authorized users only. Our CTMS offers high availability cloud computing technologies, backups and redundancy to keep the data available when you need it.
Our CTMS enforces controls for 21 CFR Part 11 compliance, seamlessly in the background as your team performs their study management activities. Controls include: audit trail, electronic signatures, data archival and user account controls.
Additional features included are eReg and eConsent.