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…
Certara2025 年 6 月 27 日
Increasing Productivity In Pharma R&D Starts With Data
This article discusses the growing volume of raw data collected during clinical research, and how…
Certara2025 年 6 月 25 日
Faster Mapping from Source Data to Target SDTM
Explore a collaborative, web-based solution for generating CDISC dataset mapping specs from standards and studies.
Certara2025 年 6 月 12 日
Pinnacle 21 Clinical Metadata Repository
With Pinnacle 21’s clinical metadata repository, you can manage your clinical metadata, the key to…
Certara2025 年 5 月 23 日
Managing Clinical Metadata for your Vendors, Studies, and Datasets
2025 年 4 月 21 日 Clinical research is witnessing an evolution, driven by the increasing complexities of…
Certara2025 年 4 月 21 日
How to Use Fix Tips for Better Clinical Data Issue Management
2025 年 4 月 15 日 Prior to submission to any regulatory agency, standardized study data is evaluated using at…
Certara2025 年 4 月 15 日
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…
Certara2025 年 4 月 8 日
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…
Certara2025 年 3 月 31 日
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.…
Certara2025 年 3 月 27 日
