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Why is it so problematic to get relevant, accurate clinical data in a timely manner?

Innoventz is dedicated to assisting clients with the development, analysis and launch of their products. Innoventz is a boutique contract research organization that specializes in medical devices. We fill the gap between a traditional CRO and a technology consultant. Our objective is to re-define the CRO role.

At Innoventz, we pride ourselves on:

  • Our comprehensive data management process utilizing trending, compliance, and error reports produces better data.
  • Our focus on clinical relevance minimizes your costs and saves you time.
  • Our high-quality customized applications and studies in Oracle Clinical results efficient data management processes.
  • Our dedication to customer service results in more successful trials.

In our experience, a well thought-out and clearly articulated data strategy is too often missing during the clinical trial planning process. A coordinated data strategy is required to accelerate the development process, reduce cycle time, and increase data quality and accuracy. Our methods of achieving this coordinated data strategy for our clients include providing Oracle Clinical Data Hosting, Clinical Data Consulting, Outcome Management and Clinical Trial Coordination services.

These service offerings allow us to deliver value to our clients:

  • We provide our clients with a study build on a stable, scalable, validated and flexible EDC or paper study data management system—Oracle Clinical (OC). By leveraging the power of the OC engine, sponsors reap the benefits of enhanced production in the research and development process to obtain efficacious, safe and cost effective products.
  • We provide our clients with a partially pre-configured data collection and extraction format based on CDISC (Clinical Data Interchange Standards Consortium) and CDASH (Clinical Data Acquisition Standards Harmonization) standards, reducing design time and establishes benchmarks for future trials.
  • We provide our clients with seamless integration of external data sources with the CDMS.
  • We provide our clients with the true benefit of focusing on higher value tasks and retaining control of the overall flow of the trial while maintaining 21 CRF Part 11 compliance.
  • We provide our clients with certified training on data management system-specific and study-specific topics, ensuring standard and efficient processes, accurate and relevant data, and reduced data management and validation cycle times.
  • We provide our clients with therapeutic and technical expertise for study build and support on OC and Medidata RAVE platforms and custom application development.
  • We provide our clients with customized data analysis and data monitoring reports as well as SAS dataset generation.
  • We provided our clients with a focus on the initial trial coordination and study build. Correct implementation of the Clinical Data Management System is essential in maintaining the primary and secondary endpoints, enrollment targets, study schedules and study budgets.

Innoventz’s mission is to maximize the effectiveness of clinical research by ensuring the successful collection, integration, and analysis of ALL data related to the clinical trial.

We are Beyond CRO. We are your partner


© Copyright 2008 Innoventz