Data Management STREAM

1. A Framework For Selecting Reliable Clinical Endpoints From Real-World DHT Data 2/25/2025

   Dr. Andy Liu presents a case study determining which digital measure of physical activity would be a well-defined and reliable clinical endpoint in a trial including patients with diabetes.

2. Make Sense Of Unstructured Data In Neurology, Urology, and Ophthalmology 5/28/2025

   Transform your data and, ultimately, patient outcomes across three major therapeutic areas: Neurology, Urology, and Ophthalmology.

3. The Cutting Edge Of Pharma: AI And RWD 1/19/2024

   Taken from a spotlight session at the CNS Summit, gain insights from thought leaders from Norstella and Citeline regarding artificial intelligence and real-world data.

4. Navigating Trials With Confidence: Building A Robust External Control Arm 12/21/2023

   Explore methods to build scientifically rigorous comparator groups to allow more patients access to life-saving treatments, accelerate trial timelines, and maximize resources.

5. Here To Help You Succeed 4/26/2023

   IQVIA Biotech is a standalone business of IQVIA with dedicated teams delivering clinical development solutions for biotech and emerging biopharma customers. Discover why IQVIA Biotech is the CRO partner of choice for biotech companies around the world.

6. Patient-Level Clinical Trial Data + Real World Data 9/6/2022

   Future-proof your clinical trial and enhance your evidence generation activities with Medidata Link, which allows sponsors to collect clinical trial data and link it at the patient level to real-world data (RWD).

7. 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.

8. Improving The Quality Of Submitted Studies To ClinicalTrials.gov 11/7/2019

   Want to reduce QC comments? Hear tips from Dr. Deborah Zarin, former director of ClinicalTrials.gov, now with the MRCT Center. Dr. Zarin was keynote speaker at the recent EXTRA: TrialScope Transparency Experience.

9. TMF Migrations: Streamlining The Journey To An Inspection-Ready Result 9/18/2023

   Delve into several techniques designed to safeguard data precision and integrity throughout the TMF migration process, reducing compliance risks and conserving valuable time and effort.

10. Improving Safety Reporting Speed And Accuracy With Automation And Embedded Intelligence 3/15/2024

    Watch this exploration of real-world case studies of companies utilizing intelligent process automation and embedded, regularly updated safety reporting regulatory intelligence of psiXchange software.