Peer-Reviewed Articles

Incorporating imaging analytics can improve the quality of work and minimize unexpected delays.

A CTC test may fulfill an unmet need in oncology clinical trials and disease management practices.

The opportunities and challenges social media provides in the realm of subject recruitment.

Building a culture of service excellence between sponsor/CROs and investigative sites.

Conversion from paper to ePRO for an instrument designed to assess diabetes' impact on quality of life.

Analysis suggests age, condition, and treatment satisfaction have most significant effect on participation.

There are opportunities to make the negotiation process more efficient and reduce timelines.

What works when and for whom in the era of comparative effectiveness research.

An efficient system can be the difference between a drug being withdrawn or delivered to market.

A quantitative approach to enhancing risk assessment and mitigation in drug development.

Systems that support automated processes have begun to transform the conduct of clinical trials.

Proper questionnaire coding and design can help set the stage for a successful trial.

Collecting PK data in late phase trials led to alleviating additional trials, drug approval, and better dosing.

Examining the challenges and solutions to the implementation of trials in resource-limited settings.

Testing cardiac safety has developed into more than measuring a simple ECG test.

Five key steps for e-submission ready documents to avoid pre-submission rework.

The disconnect coordinating and connecting interested patients to clinical trials is an ongoing struggle.

What cloud computing is, why it can save time and money, and how to select the right cloud solution.

Defining clinical trial feasibility and establishing a formula for patient recruitment success.

Application of good clinical laboratory practice reduces risks to subject safety and data integrity.

Going paperless can help an IRB quickly collaborate, share documents, and review protocols.

How to define information requirements to enhance the understanding of a clinical trial.

A review of different statistical methods for data types and models used during research.

The founding of the KKSN has helped Germany increase its clinical trial output.

The Middle East and North Africa region has seen a recent increase in clinical trials research.

The current initiatives and a historical overview of the clinical trial landscape.

Considerations in implementing a risk-based framework for computer systems validation.

Knowing when to outsource and when to conduct pharmacovigilance in-house is a crucial decision.

How bringing onboard multimodality trained personnel can impact oncology trials.

How to make the leap beyond paper and EDC to create an automated clinical environment that thrives.