Why does the FDA need to hear from patients like you?

While there is much information learned from clinical trials, they do not fully reflect the way a medical product is used in real life. Through the experiences of patients like you, manufacturers of drug and medical products can expand their understanding of a product's safety profile. In turn, manufacturers are required to inform regulators such as the FDA about these experiences. As we integrate Adverse Event Reporting across PatientsLikeMe, you will be able to help improve outcomes and safety for everyone using your particular treatment – a goal that’s at the core of the company's mission.

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