Adverse Event Reporting

FDA compliance: Adverse Event Reporting

Worldover is the quickest and easiest way to meet your Adverse Events Reporting Requirements under the MOCRA regulations. Ensure you comply with the 15 day timeline enforced by the FDA.

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Collect Adverse Event details from customers

Seamlessly capture any adverse events directly from customers into your compliance software.

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Integrated with your compliance workflow

Directly link adverse events to products

Get the end-to-end view from the event to the product compliance documentation. All in one place.

Auto link adverse event to product listing

End-to-end view of compliance

Audit trail of documentation

Instantly generate
FDA-compliant reports

We pull all the relevant information together and generate an FDA-compliance report for submission.

FDA-compliant report

Instant Generation

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Adverse Event Reporting

FDA compliance: Adverse Event Reporting

Collect Adverse Event details from customers

Directly link adverse events to products

Instantly generateFDA-compliant reports

Book a demo of our Adverse Events Reporting Tool today

Instantly generate
FDA-compliant reports