Archive: 2021
Finding the Light in a Dark Situation: Lessons Learned from the COVID Crisis
Reading Time: 3 minutesThis blog was authored by Fiona Maini, Global Compliance… Read More
How to Earn, and Keep, the Trust of Clinical Trial Participants
Reading Time: 3 minutesWhen it comes to clinical trials, no one matters more than… Read More
Leading Medical Device Company Adopts Medidata’s Remote Source Review as New Standard
Reading Time: 3 minutesMedidata’s annual global event series—NEXT Global 2021—brought together industry leaders, life… Read More
Committed to Patient Data Privacy in Clinical Trials for Life Sciences Partners
Reading Time: 4 minutesFor more than 20 years, Medidata’s customers have… Read More
Central Monitoring Is the Key to Data Integrity in Decentralized Clinical Trials
Reading Time: 3 minutesThe COVID-19 pandemic drove speedy adoption of new technologies and ways… Read More
Trust and Clinical Trial Data: A Partnership More Than 20 Years in the Making
Reading Time: 4 minutesFor more than two decades, Medidata has been in the business… Read More
How Clinical Trial Imaging Helps Tackle Disease and Assists Researchers
Reading Time: 3 minutesClinical trial images are critical as they are often used as… Read More
Medidata and Quanticate Talk Clinical Data Management and Technology in Clinical Trials
Reading Time: 3 minutesMedidata has been partnering with Quanticate… Read More
The Role of Source Data Verification (SDV) and Source Data Review (SDR) in Driving Clinical Trial Data Quality
In a risk-based monitoring (RBM) update released in January, TransCelerate defined source data verification (SDV) as “the process by which data within the case report form (CRF) or other data collection systems are compared to the original source of information (and vice versa).” Read More
The Medidata Way: Committed to Trust and Transparency in Clinical Trials
Reading Time: 2 minutesTrust. It’s a simple concept that can be hard… Read More
