|
|
 |
 |
 |
 |
 |
" As a start-up company, we have not been the easiest client to work with. In spite of challenges, they have consistently come through on their deliverable timelines with great dedication and good humor. They have continually stepped up to the bar when we have asked them for more support on the statistical side."
— Vice President of Data Management & Statistics Small Pharmaceutical Company
|
 |
|
 |
 |
|
 |
|
|
 |
 |
 |
 |
 |
 |
| Fortune Magazine rates inVentiv Health #15 of the Fastest Growing Companies. |
 |
|
|
|
 |
 |
|
 |
|
|
|
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
 |
| inVentiv Clinical provides high-quality, customized, user-friendly integration of data management and biostatistical expertise to help you efficiently collect, manage and prepare your data for approval. Our systems and processes are fully validated and 21 CFR Part 11 compliant. Our staff brings experience from more than 500 studies in all major therapeutic categories, ensuring you get what you need, when you need it. |
 |
| Our data management services are offered as part of full clinical trial services or as discrete, functional services, including: |
 |
 |
 |
| |
CRF design and printing |
| |
Database design |
| |
Double-key data entry and validation |
| |
Medical coding |
| |
Edit checks and data validation |
| |
Query management |
| |
CDISC compliant data |
| |
AE/SAE reconciliation/database |
| |
eVentiv - Proprietary EDC/eClinical technology; ability to work in multiple EDC platforms (see below for details) |
| |
Off-Shore Support (see below for details) |
|
 |
 |
|
 |
eVentiv – inTuitive EDC |
 |
| eVentiv is a proprietary, flexible validated eClinical/EDC system powered by ClinPhone. It is built on a CDISC compliant SDTM database and is 21 CFR Part 11 compliant. The eVentiv EDC system is a highly configurable software platform that adapts to your current processes and can change as your processes change. It also offers the ability to connect with other necessary applications for your study, including IVRS, imaging, and eDiaries. Our expert project teams will work with you to design the eCRF around the endpoints you need and streamline both data collection and data management processes to ensure timely and accurate data.
|
 |
Benefits of eVentiv EDC |
 |
 |
 |
| |
Combine data collected via paper and EDC in one system |
| |
Rapid installation and validation |
| |
Define flags at the CRF and item level |
| |
Automated study updates and real-time status reports |
| |
Custom notifications based on study events or actions |
| |
Custom reporting capabilities |
| |
Internal messaging system for enhanced communication |
| |
Event-driven e-mails for important study alerts |
|
 |
 |
|
 |
Off-Shore Support |
 |
| inVentiv’s experienced, English-speaking resources in Mumbai and New Delhi, India, provide added time zone coverage, accelerated ramp-up and strong, cost-effective execution for data management, statistics, programming, and medical writing projects. You can be assured of an established technology infrastructure and a team of highly trained professionals (ICH, GCP, 21 CFR Part 11). inVentiv has proven strategies for providing time- and cost-efficient solutions. For more information on our Off-Shore Solutions, click here.
|
 |
| Download our Data Management Fact Sheet |
 |
|
|
 |
|
|