5 Articles found
Formedix Articles
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Clinical data standards vs legacy data
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 ...
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Our ryze training and CDISC support services - all you need to know
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 ...
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Achieving CDISC compliance in academia
CDISC compliance is mandatory for clinical trial submissions to the US Food and Drug Administration (FDA) and Pharmaceuticals and Medical Devices Agency (PMDA). The academic world is no exception. In fact, many academic ...
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Learn how to build quality clinical studies faster at PHUSE EU Connect
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 ...
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Regulatory requirements for annotated CRFs made easy
Creating good quality annotated case report forms (CRFs) takes time and attention to detail. While it can feel overwhelming, it shouldn’t stop you. Annotated CRFs (aCRFs) are a mandatory requirement of the Food and Drug ...