Formedix
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Formedix articles

13th – 16th November 2022 | Booth #8

Are you going to be in Belfast for PHUSE EU Connect on 13th – 16th November? Do you want to learn how to build quality clinical studies faster and easier?

Then let’s connect!

Nov. 2, 2022

Creating good quality annotated case report forms (CRFs) takes time and attention to detail. While it can feel overwhelming, it shouldn’t stop you. A

Whether you’re a regular ryze user or are new to the platform, at some point you might need some help navigating your way around. From product training on the ryze platform to support with a specific element of the CDISC standards, we’re here to he

Dec. 1, 2022

Data standards are a feature of many regulated industries, and the pharmaceutical industry is no exception. But we didn’t always have standards to help us collect, analyze and submit data. Even today, some organizations are not utilizing industry or company standards to ensure their study data is collected the same way every time - despite the many benefits of standardization.

Why are some organizations slow to adopt change?

Dec. 2, 2022

CDISC compliance is mandatory for clinical trial submissions to the US Food and Drug Administration (FDA) and Pharmaceuticals and Medical Devices Agency&nb

Nov. 2, 2022

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