Founded in 1999, IntegReview IRB meets customer demands by providing daily IRB meetings, secure online 21 CFR Part 11 compliant document management system, 24-48 hour turnaround for U.S., Canadian, Latin American and Japanese review, as well as prompt, thorough, responsive and professional service.
Provides IRB review for all phases of research in multiple therapeutic areas.
Exemplary customer service. You can always reach someone if you have questions.
The company is woman-owned and AAHRPP accredited.
Save time and simplify your regulatory tasks with Complion, the industry’s leading eRegulatory solution designed to make your life easier.
• Eliminate paper binders
• Collect eSignatures
• Track expirations and outstanding tasks
• Ensure 21 CFR Part 11 Compliance
• Standardize filing and naming conventions
• Simplify remote monitoring
Experience the Complion Difference
• Trusted by 80+ sites to manage over 4,000 studies.
• Accessed by 1400+ monitors from 170+ sponsors and CROs!
• The only system designed to automate repetative tasks
• Best practices and industry standards
• Template policies and SOPs to ensure your long-term success
• Maximize sponsor acceptance and reimbursement
• Largest and most experienced team on the market
Sign up for a free demonstration today!
The Leader of Global Clinical Trial Management Sytems
RealTime Software Solution is a global leader in SAAS-based Clinical Trials Management Systems for Sites, Sponsors, and CROs. RealTime is also the only CTMS vendor that can offer a complete suite of solutions into a seamless platform, SOMS (Site Operations Management System).
SOMS includes the industry-leading CTMS, SitePAY, TEXT, eDOCS, and eSOURCE which is accessible through an easy-to-use MobileAPP. RealTime also has the most advanced multi-site and site network enterprise systems available anywhere.
With an international customer base, multiple integrations with other vendors, advanced recruitment systems, intuitive monitoring portals, Outlook integration, a powerful MobileAPP and more; the team at RealTime has made a significant impact on the efficiency of the clinical research process from start to finish.
Our History
RealTime-CTMS was initially developed in 2005 by experienced clinical research professionals. Today, the leadership and stakeholders of RealTime Software Solutions are some of the most prominent knowledge and opinion leaders in our industry. RealTime will continue to expand its service offerings and the delivery of disruptive new technologies that will shape the future of clinical research.
Syneos Health is the only fully integrated biopharmaceutical solutions organization. Our company, including a Contract Research Organization (CRO) and Contract Commercial Organization (CCO), is purpose-built to accelerate customer performance to address modern market realities. Created through the merger of two industry leading companies – INC Research and inVentiv Health – we bring together more than 21,000 clinical and commercial minds with the ability to support customers in more than 110 countries. Together we share insights, use the latest technologies and apply advanced business practices to speed our customers’ delivery of important therapies to patients. To learn more about how we are shortening the distance from lab to life visit SyneosHealth.com.
Bio-Optronics is the creator of Clinical Conductor (CC CTMS), known for generating significant savings with its robust finance capabilities, it is also the leading CTMS for executing collaboratively across multiple clinical trials and sites, including enabling remote workflows. Used by more research sites around the world than any other CTMS, Clinical Conductor is currently managing over 40,000 studies, including a significant percentage of the world’s COVID-19 clinical trials.
CC CTMS is part of the CCTrialSuite, a comprehensive set of integrated, patient-centric clinical research management products that together streamline research operations while maintaining a high degree of compliance. Complementing Clinical Conductor in the suite are several remote workflow enabling solutions. CCPay offers sites the unprecedented ability to both control finances and improve patient satisfaction with real-time payment reimbursements using secure pre-paid payment cards, all controlled remotely from CC CTMS dashboards. While CCText, the only fully CTMS-imbedded, conversational 2-way text messaging solution, has demonstrated clear results with increased patient recruitment, engagement and retention. An expanding set of remote workflow capable solutions include Part 11 compliant CCeReg document management, remote monitoring enabled CCeSource data capture, mobile friendly CCeConsent, and easy to engage remote visits using the HIPAA compliant CCVideo solutions from a single SaaS supplier, Bio-Optronics.
Click here for free access to The Ultimate Guide to Clinical Trial Software!
Also visit www.bio-optronics.com or follow @BioOptronics on Twitter or LinkedIn
Scientific teams require highly specialized skill sets that are in higher demand than ever before. The talent skills gap is real, and regulations across a wide range of scientific settings require an expert workforce.
Since 2009, Medix’s Scientific Division has connected scientific teams with highly skilled and sought after talent. As the numbers of registered clinical trials in America rose rapidly in the following years, Medix Clinical Research was founded in 2013 to service sites, sponsors and CROs of all shapes and sizes. In 2015, Medix Clinical Research introduced client consulting, bringing a more personalized approach to the site experience by providing expert guidance.
Today, our team supports scientific clients with staffing, workforce solutions and consulting in Clinical Research Sites, Pharmaceutical/Biotechnology, Medical Device and Food & Beverage
The increased demand for clinical research trials has created talent imbalances for sites, leading to staff dissatisfaction, financial instability and, ultimately, lower quality trials. Through our best-in-class recruitment services and proprietary behavioral assessment, we will deliver talent who match your needed hard skills, soft skills and cultural fit. Every site’s needs are different, so whether it’s operational or compliance based, our in-house clinical research staff is dedicated to help your site build a sustainable research program.
Medix Clinical Research offers a full range of staffing, consulting and workforce solutions for clinical research sites, including:
Site Operations
Finance (Budget and Contracting, Revenue Collection Cycle)
Compliance
Recruitment and Retention of Talented Staff
Clinical Research Boot Camp, powered by ACRP
For more information, please visit www.medixteam.com, or contact us at 1-866-44-MEDIX.
