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Oracle® Health Sciences Adverse Event Integration Pack for Oracle Health Sciences InForm and Oracle Argus Safety Implementation Guide
Release 1.0.1

E36157-02
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Preface

The Adverse Event: InForm and Argus Safety integration automates the process of clinical study sites reporting serious or clinically significant adverse events for a drug or a medical device from Oracle Health Sciences InForm to the Oracle Argus Safety system.

Audience

The audience for this Implementation guide is database administrators (DBAs) and system administrators implementing the integration. If you want assistance with implementation, engage Oracle Consulting.

Documentation Accessibility

For information about Oracle's commitment to accessibility, visit the Oracle Accessibility Program website at http://www.oracle.com/pls/topic/lookup?ctx=acc&id=docacc.

Access to Oracle Support

Oracle customers have access to electronic support through My Oracle Support. For information, visit http://www.oracle.com/pls/topic/lookup?ctx=acc&id=info or visit http://www.oracle.com/pls/topic/lookup?ctx=acc&id=trs if you are hearing impaired.

Related Documents

For more information, see the following documentation sets:

Oracle Health Sciences Adverse Event Integration Pack for Oracle Health Sciences InForm and Oracle Argus Safety

Oracle Application Integration Architecture

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