Most clinical trial managers and CROs only focus on data collection objectives rather than data analysis and study outcome objectives - including planning for the integration of data. Trial data needs may not be fulfilled by a Clinical Data Management System (CDMS) alone. Innoventz offers a coherent data strategy that consists of a coordinated process of Clinical Trial Coordination, Clinical Data Consulting, Outcome Management, and Oracle Clinical Data Hosting and Services to produce valid trial data.

Clinical Trial Coordination is the methodology of ensuring the trial is set-up correctly in the early stages of the trial. Our efforts begin with developing a strategy fro trial design and trial management by analyzing the protocol and developing the Data Management Plans (DMP) and Standard Operating Procedures (SOP), as well as training all members. Although Clinical Trial Coordination begins at study start, it is continued throughout the course of the study by maintaining the processes.

Oracle Clinical Data Hosting and Services encompasses any Oracle Clinical study build and support. We provide a set of CRFs that are CDASH (Clinical Data Acquisition Standards Harmonization) and CDISC (Clinical Data Interchange Standards Consortium) compliant that can be customized to meet your study needs. Innoventz can host your data on our validated Oracle Clinical installation or our consultants can work with you on your own Oracle Clinical infrastructure to provide process improvements, a flexible and scalable platform, standards compliancy, data integration, complex edit checks, reporting and analysis all on a centralized database.

Any CRO can collect, store and manage data. But if that data isn’t high quality, your entire trial could be in jeopardy. This is where Innoventz can help you reach the next level.

Our work starts before the database development and data collection process begins. We anaylyze your protocol in order to design and implement CRFs, Data Validation Specification, eCRF Specification, Data Management Plans and SOPs. After we have completed an analysis of your study requirements, we develop a comprehensive and coordinated data strategy that integrates all data sources and trial conduct management.

Innoventz provides a unique blend of strategic consulting and CRO services. Our level of expertise in data hosting, Oracle Clinical, Medidata RAVE, SAS and other systems is so extensive that we prevent costly errors and logistical mistakes.

Our team of experienced software developers produces leading-edge, innovative customized software solutions to enhance and meet the unique data management, trial management, reporting and analytical needs of your company while providing you more customization and control of your study.

Innovative, strategic solutions – ones that proactively tackle data and process issues – make Innoventz an integral asset to the success of your trial.

With Innoventz, you eliminate the high costs of poor quality data, redundant data clean-up efforts and, in worst case scenarios, a failed trial. Just as importantly, when we manage your trial data, you have more time to focus on research and critical macro-level decisions for your company.

Our dedication to customer service sets us apart from other CROs. Good customer service is an integral part of our value proposition, which combines our service offerings, our performance, and our pricing. We provide answers to your needs while providing a cost-effective and strategic solution in a timely and professional manner. Ultimately, with Innoventz as your trusted CRO partner, you not only obtain better quality data, minimize costs and save time, you achieve more successful trials.

60% of all new trials (Phase I - III) are expected to use EDC in 2008. Spending on EDC solutions will total more than $3.1 billion for 2006 - 2011. Currently, there are many EDC options available. The rapid growth in the industry can make it difficult for a small or mid-size company to transition from a paper study to an EDC-based study. In our experience, the type of EDC platform you choose is not always the most important decision. The correct implementation of the study on that platform is the most important task that can affect the growth and success of your study.

With our clinical experience in a wide range of therapeutic areas, we are able to provide cost-effective and strategic EDC solutions for our clients. Our study build cost analysis and service offerings are flexible and scalable to meet your study needs.