Clinical Data Solutions

Clinical trial sponsors, as well as Contract Research Organizations (CROs) and Academic Research Organizations (AROs), are ever-diligent about meeting the demands and complexities of developing and managing clinical trials in the safest possible manner. At the same time, they continue to seek ways to optimize trial success rates, improve operational efficiencies, and increase their return on investment. By adopting industry-leading technology solutions, these organizations have found an effective and more predictable means of streamlining processes, reducing cycle times, decreasing expenditures and gaining earlier access to the data they need to make informed decisions.

Building on our innovative technology platform, MedChannels develops and markets data collection and management solutions that enable bio-pharmaceutical companies, medical device companies, CROs, and AROs to integrate and automate the management of their entire clinical development process. As a pioneer in web-based electronic data capture (EDC) and clinical data management (CDM), MedChannels is fundamentally transforming the way clinical trial data are collected, analyzed and managed. With the addition of applied data standards technology MedChannels delivers the comprehensive clinical trial solutions needed to track product efficacy and safety – from study initiation through FDA submission.

	EDC: OrderPro™
	Advanced Electronic Data Capture (EDC) technology incorporates streamlined study design, workflow, discrepancy management, coding, integration standards, regulatory compliance, and extensive reporting and analysis into the overall solution... read more
	CDM: TrialPro™
	Clinical Data Management (CDM) means maintaining compliance with industry and government regulations. The TrialPro product offers a complete set of features for streamlining data entry and lab loading, discrepancy management and resolution, patient and site reporting, data exporting, coding and system administration... read more
	ADS: netSDTM™
	The web-based Submission Data Trial Manager (netSDTM™) application allows users to load CDISC's SDTM-compliant study data, check and correct errors and inconsistencies, and browse data in a variety of tabular and graphical formats. The netSDTM product allows companies to ensure that submission files conform to Applied Data Standards (ADS) so that they can present them to regulatory agencies with confidence... read more