ClinTech Articles

Key Considerations for the Adoption of eConsent for Sites

By Sandra SAM Sather

There are many benefits for sites adopting electronic informed consent and it is vital that site study teams are not bystanders in the move towards its use.

Building Quality into Study Startup

By Craig Morgan

The ICH-GCP E6(R2) includes a section dedicated to risk-based Quality Management, and states that the sponsor should implement a system to manage quality throughout all stages of the trial process, including the beginning.

Study Sites Indicate eSource Improves Data Quality

By Moe Alsumidaie

The challenges of data quality are a constant factor in clinical trials, especially that of traditional paper source documenting. Joyce Smith of The Medical Research Network speaks about the study’s site perspective on trial data quality.

Introduction to Cloud Computing for the Analysis of Large Human Datasets

By David Hall, PhD

The economics and power of the cloud will drive its increasing adoption by pharma organizations for the foreseeable future as research becomes more data-intensive.

How to Leverage Big Data to Improve Clinical Site Selection

By Suzanne Caruso

Predictive modeling has allowed biopharma companies the opportunity to solve inaccurate, inefficient and misinformed site selection practices by leveraging big data.

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