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Presentation

My eReport PM (also called My eReportStudies) is the Post-Market Studies version of My eReport. It facilitates the reporting in a dedicated database of all cases related to PASS/PAES studies (Post-Marketing studies - Phase 4 studies) initiated after the marketing authorization of a drug. Users participating in this type of study will send their cases directly to the laboratory that initiated the study.

My eReport PM boosts a product while monitoring the potential risks that can be created. This is the link allowing the Marketing and Pharmacovigilance departments to work together.

Screenshots




Specifications

My eReport PM can be used on a mobile device running iOS (iPhone, iPad) or Android (Samsung, Huawei...). A version is also available as a web form accessible from any type of computer with an Internet connection.

Application primarily European, My eReport PM is translated into 7 languages : French, English, Spanish, German, Dutch, Czech, Portuguese, Italian and Romanian.

We customise the data form for your My eReport PM application based on your post-market studies.

My eReport PM contains advanced features like the ability to take a photo of the medicine packaging, its medication guide, or the side effect. A QR code scanner is also integrated to quickly retrieve the drug information (trade name of the drug and laboratory name).

An anonymized copy of your report is automatically sent to the relevant health authority (Regional CRPV for France, National Agencies for foreign countries). You can also receive, by specifying your e-mail address (not kept), your own copy of your report.