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SAE Reconciliation

Easily Review and Compare Serious Adverse Events (SAEs) Data in from your Clinical and Safety Databases with our configurable GxP-Compliant Validated Software

With eReconciliationĀ®, manage your safety data reconciliation and adverse event reconciliation operations easily and efficiently: review data from one or more sources, create groups of data items, display data sources side-to-side on the same screen, monitor changes in source data, produce reports and keep track of user actions.

Why is Safety Data Reconciliation so Important? 

Because in clinical trials safety information is collected from more than one source and stored in more than one places, discrepancies can emerge between the databases and must be reconciled or documented so that data submitted to regulatory authorities are validated.

eReconciliation for SAE Reconciliation Management

Safety Data Management Glossary and Tools

A list of terms and definitions related to Serious Adverse Events, adverse event data management and SAE Reconciliation.

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eReconciliation for SAE Reconciliation

SAE Reconciliation Handbook

Download your FREE practical guide on how to reconcile safety data stored in more than one databases.

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eReconciliation for Safety Data Reconciliation: Operation Oversight

SAE Data Management EMA & FDA Regulations

The quality of safety data collection and reporting is paramount to the establishment of a drug safety profile. Here are helpful links to the EMA and FDA regulations addressing those concerns.

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Download Your SAE Reconciliation Handbook (16 pages)

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SAE Handbook Download

Download your FREE practical guide on how to reconcile safety data collected from various sources and stored in more than one databases.

Download your complete safety data reconciliation handbookREAD MORE

Clinical Safety Glossary

A list of terms and definitions related to Serious Adverse Events, adverse event data management and safety and clinical databases SAE Reconciliation.

Check Now the Safety Data Reconciliation GlossaryREAD MORE

Pharmacovigilance Regulations

The quality of safety data collection and reporting is paramount to the establishment of a drug safety profile. Here are helpful links to the EMA and FDA regulations addressing those concerns.

Safety Data Reconciliation: check now EMA and FDA Regulations & GuidelinesREAD MORE