Did you know…

The collection and processing of adverse event information requires many steps by individuals with special training in pharmacovigilance. The manner in which these steps are executed are dictated by regulations. Each country or geographical area are governed by regulatory authorities. Each of these regulatory authorities, where a product is marketed, determine how and when qualifying adverse event information gets reported. Because of the complexity of getting this right, pharmaceutical companies often rely on external vendors like us to perform daily or periodic regulatory reporting tasks on their behalf. Let Med Communications team of experts guide you will all of your pharmacovigilance needs. We are here when you need us!

Contact us to discuss how we can assist with your pharmacovigilance needs: 877-477-0977 or

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