Data Management and Analysis
Transforming Clinical Trials
Harnessing wearables for Real-World Data (RWD) and Real-World Evidence (RWE) collection and analysis
Clinical trials are at a pivotal juncture in For decades clinical trials have largely relied on controlled environments
Getting The Most Out of Your Clinical Trial
Collecting human factors data to improve commercial device design
Human factors engineering HFE is crucial in developing an effective device and is critical to meeting global regulatory expectations
FUTURE OF CLINICAL TRIALS IN APAC
Oracle’s initiative
We are seeing pharma shift to explore newer clinical trial models and technologies
THE AGGREGATE SAFETY ASSESSMENT PLAN
A valuable tool for clinical trial safety planning
Recently a Drug Information Association American Statistical Associationsponsored Interdisciplinary Safety Evaluation working group published a recommended approach to the aggregate assessment of clinical trial safety data
EMPLOYING REAL-WORLD EVIDENCE TO IMPROVE CLINICAL TRIAL STRATEGIES
There are many advantages to studying a drugs performance under everyday conditions that cannot be matched in clinical trials which are essentially controlled experiments A traditional Randomised Controlled Trial RCT which has a specific design with established inclusion and exclusion criteria cannot anticipate all the realworld situations that can...
