Dec 12, 2022 Introduction to software as medical device (SaMD) By Liat Laufer Digital tools and applications have become integral parts of our daily lives.... Learn more
Dec 12, 2022 Conceptual controversies in the use of the terms “gender” and... By Fadwa Dabbah In the past, scientists often used only male subjects for experiments (females... Learn more
Dec 07, 2022 The QC Process for CSRs By Danielle Hadar When starting QC work on a document, I first look through the... Learn more
Jun 17, 2021 Using Risk-Based Monitoring To Focus On What Matters Tanya du Plessis, VP Data Solutions and Strategies at Bioforum and Rich Davies, VP Solutions... Learn more
May 06, 2021 Tips For Writing a Winning Grant Proposal Writing a winning grant proposal is not an easy task. This series of tips aims... Learn more
Jan 13, 2021 Writing a Clinical Study Protocol as a Regulatory Document A few years ago, when I was a staff member in a clinical research site,... Learn more
Nov 12, 2020 Overcoming the Paradox of Choice: Selecting EDC Capabilities to Fit... In partnership with Applied Clinical Trials, our VP of Data Strategies & Solutions Tanya du... Learn more
Oct 21, 2020 The Cost of Queries, Reduce the Burden, Risk based Data... In general, increased industry costs are driving n to reflect on current practices in order... Learn more
Oct 07, 2020 Risk based Data Management, nay targeted data review There is no doubt that our clinical trial designs are getting more complex by the... Learn more
Apr 07, 2020 A “Rescue” Study Doesn’t Have To Be Daunting: Six Best... No clinical trial sponsor intentionally plans a study migration. Sometimes the decision to migrate data... Learn more
May 06, 2019 Data managers in a changing technological landscape Technological advances, providing better and quicker way for collecting increasing amounts of data, pose a... Learn more
Feb 20, 2019 AI in data management Growing amounts of collected clinical data augment the importance of reassessing the methods used for... Learn more