ClinTech Articles

May 18, 2017
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.
May 11, 2017
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.
Mar 07, 2017
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.
Feb 16, 2017
Predictive modeling has allowed biopharma companies the opportunity to solve inaccurate, inefficient and misinformed site selection practices by leveraging big data.
Jan 24, 2017
While wearable devices are mainly an advantageous way to collect data from monitoring a trial participant’s progress, there are scientific and operational considerations to be aware of.
Jan 20, 2017
The Expert Determination standard of protecting patient privacy can answer the growing demand for better data for research and analytics in healthcare.
Jan 12, 2017
Traceability plays a crucial role in ensuring the integrity of source data and in reinforcing clinical research results. CDISC has developed Trace-XML as an extension of its Define-XML model for delivering clinical data lifestyle traceability from data collection through to final analysis.
Dec 02, 2016
A new SaaS platform for clinical trials, soon available to all pharma companies, aims to automate clinical supply, improve patient compliance and enable better medication adherence.
Sep 12, 2016
Investment in mHealth and the adoption of wearables are significant initiatives that are changing the clinical trial process toward a more patient centered approach. These wearable technology initiatives have the potential to be the most innovative advances in drug development.
Aug 12, 2016
With the healthcare industry’s transition from paper to digital, verification is changing beyond that of a signature in ink. Electronic signatures are a new medium in clinical trials that the industry is now turning to in this transition to digital.
native1_300x100
lorem ipsum