The Do’s and Don’ts of Define.xml
Discover the 6 dos and don’ts of creating compliant define.xml files for FDA submission with…
CertaraJune 27, 2025
Faster Mapping from Source Data to Target SDTM
July 15 - 11am ET & July 17 - 11am IST
CertaraJune 12, 2025
Pinnacle 21 Clinical Metadata Repository
With Pinnacle 21’s clinical metadata repository, you can manage your clinical metadata, the key to…
CertaraMay 23, 2025
Managing Clinical Metadata for your Vendors, Studies, and Datasets
April 21, 2025 Clinical research is witnessing an evolution, driven by the increasing complexities of…
CertaraApril 21, 2025
How to Use Fix Tips for Better Clinical Data Issue Management
April 15, 2025 Prior to submission to any regulatory agency, standardized study data is evaluated using at…
CertaraApril 15, 2025
Standardizing Real World Data in Rare Disease: ATHN’s Journey
Learn how Certara helped ATHN standardize Real World Data for regulatory submissions, advancing rare disease…
CertaraApril 8, 2025
How to Make 3rd Party Reconciliation in Clinical Data Management More Efficient
Learn how to streamline 3rd party reconciliation in clinical data management with reusable standards, centralized…
CertaraMarch 31, 2025
The Revolution of Metadata Standardization with Clinical Metadata Repository (CMDR)
Solution Consultant, Software, APAC (Japan) Rico Fujita is a Software Solution Consultant in Japan, APAC.…
CertaraMarch 27, 2025
Exploring Common CDISC ADaM Conformance Findings
March 27, 2025 ADaM data are required by the FDA and PMDA and accepted by…
CertaraMarch 27, 2025
