How to Automate CRF Annotations – A Best Practice Guide
This free guide explores how to automate CRF annotations, the benefits of automation, and the…
CertaraOctober 24, 2024
How to Use CDISC’s ODM Standard for CRF Design
Over the last decade, our industry has become familiar with Clinical Data Interchange Standards Consortium…
CertaraSeptember 25, 2024
Regulatory requirements for annotated CRFs made easy
aCRFs are a mandatory requirement of the FDA, and therefore a key submission deliverable for…
CertaraAugust 26, 2024
A Best Practice Guide to CRF Design
Design quality, effective and reusable case report forms with our CRF Design Guide. Download the…
CertaraJune 7, 2024
Everything You Need to Know About CRFs in Clinical Trials
Read about the basics of CRFs and eCRF design, why annotated CRFs should be standardized…
CertaraMarch 26, 2024
Formatting Annotated Case Report Forms (aCRFs): Not Submitted Annotations and SDRG
Simplify aCRFs with insights on “Not Submitted” annotations, reviewer’s guide tips, and define origin column…
CertaraNovember 13, 2020
Formatting Annotated Case Report Forms (aCRFs): Multiple copies and/or multiple versions of forms
Streamline aCRF formatting by mastering versions, repeated pages, and compliance essentials. Read the third blog…
CertaraOctober 9, 2020
Formatting Annotated Case Report Forms (aCRFs): Document properties, bookmarking and table of contents
Discover essential tips for formatting annotated CRFs, from dual bookmarking to document properties. Read the…
CertaraSeptember 10, 2020
Formatting Annotated Case Report Forms (aCRFs): Part 1
Discover essential tips for formatting aCRFs with clarity and regulatory compliance in mind. Read the…
CertaraAugust 12, 2020
