very clinical researcher understands the importance of saving time and resources during the conduct of clinical trials. This is especially true when you consider the collection, processing and management of protocol-specific data for each study subject. In the past, study coordinators relied on paper Case Report Forms (CRFs) to ensure the required patient data was recorded and transferred to the sponsor for processing and analysis.

Thankfully the days of paper CRFs are largely behind us as the industry understands that the use of electronic data capture (EDC) systems increases the efficiency of data collection and improves overall data quality. In addition to increased speed and quality, EDC also provides faster data access, improved security and greater visibility while reducing costs and ensuring regulatory compliance. All EDC solutions are not created equal so selecting the right one is very important. Your EDC system should be flexible, highly-configurable, scalable, easy to use and, most importantly, compliant with all requisite regulatory requirements and industry standards.

Ennov EDC is a comprehensive clinical data management solution that allows clinical research personnel to easily define EDC studies and collect subject data without the worry of missing or inaccurate data. Ennov EDC is easy to use and supports the design, deployment and capture of multi-center clinical trial data within one flexible and scalable solution. Our software supports clinical trials of any size, including large global trials, post-marketing trials, cohort trials, health surveillance, Phase I-IV trials and epidemiological trials. Ennov EDC facilitates complete and accurate data collection and improves communication within clinical teams.

Features:

• Streamlined clinical data capture

• Requires no IT or programming skills

• Increased data visibility and security

• Medical coding for MedDRA and WHO Drug

• CDISC, CDASH and SDTM compliant

• Full web interface

• 21 CFR Part 11 compliant

• Available in the App Store

• Compatible with existing Ennov Clinical studies

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