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Dermatology Studies: Accelerate Your Builds

Solution Sheet

We recognize that each clinical trial has unique needs, and adopting eClinical software that meets those needs is a clear organizational asset. With an overall customer satisfaction rating of 98%, our eClinical platform has been used in over 50 dermatology studies by more than 12 organizations- including Innovaderm Research, Altasciences, and Precision Medicine Group. Here are a few key reasons why we are a trusted solution for Dermatology trials:

Feature Functionality with Medrio

File Attachments

Attach photos and other records to Medrio EDC for consistent visibility into topical reactions.

Dictionary Coding

Report adverse events with precision so you can act on them more quickly.

Rapid Study Startup

Build databases in days with no programming required, and keep your studies moving quickly.

How Do Our Solutions Help?

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EDC

We have achieved notable success in supporting dermatology researchers with robust feature functionality. File attachments allow researchers to upload photos and other records directly to the EDC for consistent visibility into topical reactions. Additionally, dictionary coding permits users to report adverse events quickly and precisely – making it easier to take any necessary action without delay.

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eConsent

We can help you accelerate form setup and deployment of changes. It’s also highly effective for facilitating better patient comprehension with graphics and videos. This empowers you to spend less time and resources clarifying consent forms while improving patient retention and reducing recruitment efforts.

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ePRO

You can empower patients to report their experience electronically, in their own words, and from the comfort of their home – helping you to reduce participant burden and strengthen patient engagement.

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DDC

Capture data from the source, sync directly to EDC, and further facilitate data collection in-clinic or in the field. Boost data quality by catching errors quickly with real-time edit checks, reduce transcription errors by eliminating paper from your data entry process, and make your overall monitoring efforts more efficient and productive.

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RTSM

We know randomization can make or break a study. What if a single solution could help you reduce site overages by 20 – 40% while increasing patient compliance and meeting all of your randomization needs? It would be a game-changer, and we’re here to tell you–we’ve changed the game.

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