How the merging of medical faculty and academic hospitals in The Netherlands is improving the country's research infrastructure.
Industry news focusing on the people and organizations who work in the clinical trials profession.
Surveys among pharma, clinics, and investigators shed light on trials in children.
Outsourcing fundamentals for this pick-and-choose model so that both sponsors and service providers win.
Finding a strategic approach to writing clinical study reports.
Mick Ryan, vice president of IT at ICON plc, discusses the growing use of artificial intelligence in clinical research—from technology and data analysis to patient privacy and ethics.
Collaboration and regulation were the watchwords at DIA Global this year, where the ICH E6(R3) guideline, published in final draft form in May, was the talk of the congress.
Undertaking an assessment of the POS can be coupled with the product profile and safety assessments of compounds prior to launching a clinical trial.
Effective ways for sponsors to reduce risk when embarking on comparative clinical trials.
Perspectives on adoption of technology at U.S. Academic Medical Centers and how sponsors will be impacted.
Integrating clinical trials and named patient programs to provide global access to drugs before approval.
Approaches such as machine learning, AI and neural networks are still in their infancy, but with AI companies rewriting the code for drug discovery, the implications in pharma are likely to be far ranging in the coming years.
Instinctively, when there are more investigators/sites being deployed for a trial with a defined number of patients needed, we should expect shortened enrollment cycle time. This sounds right, but is it really?
An integrated product development plan designed early increases the odds of on time success.
Launched in 2003, the LCN Project calls for more studies and an improved trial infrastructure.
Sponsors are responsible for monitoring studies, patient safety, and data integrity.
Launched in 2003, the LCN Project calls for more studies and an improved trial infrastructure.
Tracking the life cycle of a drug is a complex process that early planning and IVR technology can help ease.
Using a specific trial, the importance of assessing the success of therapy masking is examined.
This is the third post in a three-part series on quality implications of RBM.
The temptation to use uncontrolled, early, small studies to support further development of products may prove problematic for emerging biopharma companies.
Launched in 2003, the LCN Project calls for more studies and an improved trial infrastructure.
In this Web-based strategy, suppliers bid "down" prices for the privilege to sell their products and services. Is big pharma sold?
In this Web-based strategy, suppliers bid "down" prices for the privilege to sell their products and services. Is big pharma sold?
Launched in 2003, the LCN Project calls for more studies and an improved trial infrastructure.