Compliance Management

The ExtraView platform may be configured for many different aspects of compliance management systems. The product's unique configurability, allows it to adapt simply to many business processes such as quality tracking, adverse event reporting and the tracking of calibration events. Featured below is the Adverse Event Reporting system.

Adverse Event Reporting


ExtraView Adverse Event is a web-based adverse event management and reporting system that features unprecedented flexibility and ease of use. Used by the world’s largest medical device and pharmaceutical companies, ExtraView is the foundation for global capture, analysis, and resolution of adverse events related to medical device, treatment and diagnostic systems.


“Early identification and reduction of potential risk is a key benefit of an adverse event reporting system.”
--Alfonso Serrato, President & CEO, BioRes Medical Inc


Platform-independent and highly scalable, ExtraView Adverse Event may be quickly customized for any workflow and product development process.



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Features Overview
WEB-BASED True global access & administration from any site, anywhere on the Web
UNLIMITED ATTACHMENTS Immediate or gradual replacement of paper-based systems
FDA 21CFR
PART 11
Full compliance with FDA requirements electronic records, electronic signatures
WIRELESS Access & update any record from meetings, sites, etc.
NOTIFICATION SYSTEMS Smart notification systems with filtered data and hotlinks
SUPERIOR REPORTING Medwatch and other reports in Excel, Word, PDF, Charts, text, HTML, XML
OPEN INTEGRATION API and CLI are language independent and use HTTP, XML, and other
open standards

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