Data Management STREAM
-
5 Strategies To Dramatically Improve Clinical Data Quality
10/29/2024
Discover how to unify data management and risk-based quality management approaches and augment processes with automation and AI to find and fix data quality issues sooner and more efficiently.
-
Citeline Study Feasibility
11/30/2021
This predictive analytic solution helps sponsors select global study sites to successfully enroll more patients and accelerate clinical trial cycle times. Study Feasibility leverages both human expertise and machine-learning algorithms trained on Citeline’s best-in-class data.
-
Helping Sponsors Keep Up With The Latest Clinical Trials Intelligence
11/11/2022
Trialtrove helps sponsors form development strategy, anticipate competitive activity, benchmark trial designs and analyze trends. Sponsors also enjoy direct access to industry-leading analysts.
-
Medidata Clinical Data Management
4/24/2024
By automating complex tasks, Medidata Rave simplifies clinical data management and capture. This leads to cleaner, more reliable data, allowing for quicker analysis and results.
-
Why Veeva CDB
6/24/2024
Watch a two-minute video to learn how Veeva Clinical Database (CDB) aggregates, cleans, and transforms clinical data from various sources, including third-party EDCs.
-
How To Supercharge RWE Generation In Phase IV Trials
8/11/2023
Watch as speakers discuss their joint efforts in implementing patient-centric digital trial solutions that harness the potential of RWD, translating it into actionable Real-World Evidence insights for a sponsoring client.
-
Keeping Up With ClinOps: Why And How To Improve Delivery
11/6/2023
Industry experts discuss the concept of a trial platform as a service and how it can accelerate and enhance the day-to-day functions of clinical operations throughout the entire lifecycle of a study.
-
ETL: Maximizing Reuse Of Your Clinical Trial Data
5/6/2019
ETL — extract, transform, and load — enables sponsors to operationalize clinical trial data, leverage off the investment they have made in other sources to reuse data, and automate populating key elements for registration on CT.gov and EudraCT.
-
Harnessing The Potential Of Patient-Level Data In Clinical Trials
6/19/2024
Join our panel of industry leaders as they explore innovative methods and best practices for incorporating fully consented patient data in clinical trials.
-
Beyond Clinical Trial Disclosure – The Ethical And Business Demands For Clinical Trial Transparency
11/4/2020
The COVID-19 pandemic brings to light the ethics of getting information out more quickly than strictly required by regulation, or more thoroughly, as medical professionals, media and the general public are all looking for effective and safe treatments.