Managing Adverse Events (AEs) During Fieldwork

We combine a robust and secure platform with compliance principles to deliver a seamless experience in monitoring and reporting AEs.

Adverse Events (AEs)

Partner with us on medical products and device market research, and make the most of our reliable monitoring and reporting system.

Our team of experts, supported by advanced monitoring technology, diligently check responses on a daily basis to ensure that nothing is missed.
By drawing upon years of expertise in healthcare market research, we have developed the ability to prioritise timely report generation without compromising on quality.

The m360 Research Difference

Share with us your reporting obligations, and we’ll make sure your requirements are incorporated in our project plans.

Frequently Asked Questions (FAQs)

An adverse event (AE) is any untoward medical occurrence in a patient or clinical investigation subject administered a  pharmaceutical product and which does not necessarily have a causal relationship with this treatment.

Monitor and measure occasional harm from medication and whether the risk-benefit ratio is high enough to  continue use of any particular drug.

AE notifications should be reported within one working day (24h) and if the data is collected over weekend, it can be reported on the next working day, within one business day of the team becoming aware of the AE.

Healthcare professionals and consumers, pharma companies, people or companies working for MAHs (Marketing Authorization Holders), the sponsor, or sub-contractors of the MRA.

An identifiable patient, an identifiable reporter, product exposure, and a specific event.

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What are your AEs requirements?