Filip Matakovic, MedPoint Digital

Regulatory Binders: Your Path to Paperless

PAID MESSAGE - Save to PDF, print, copy, file, repeat. Sound familiar? For those handling and managing the regulatory documentation at clinical research sites, it's a common workflow full of paper and redundancy. Maintaining a Regulatory Binder is a task that hasn't changed much over the years. Stacks of documents, protocols, amendments, IRB approvals, correspondences, […]

Leverage Clinical Trial Participant Feedback to Boost Performance

With the touch of a few computer keys you can tell the world via platforms like Yelp that a vaunted local brew pub’s seasonal draft is flat, a hotel’s beds are lumpy, and the pricey luggage set you just purchased at a certain upscale department store looks more worn out than you after just a […]

Clinical Trial Industry Urged to Tackle PI ‘One and Done’ Problem

Chronic principal investigator (PI) turnover and shortages will continue to hold the clinical trial industry back until we do a better job educating and training vital new entrants, says Christina Brennan, MD, MBA, vice president for clinical research at Northwell Health Feinstein Institute for Medical Research. “It’s a real problem in our industry.” The so-called […]

Jim Kremidas, Executive Director, ACRP

Oracle Survey Finds Investigative Sites Still Frustrated with eClinical Technology

"Sites are overwhelmed with too many solutions and ballooning login credentials," said Jim Kremidas, executive director, ACRP. "Instead of engaging with patients, an inordinate amount of time is spent learning new systems, completing redundant required training and reentering the same data multiple times. Simultaneously, pharmaceutical companies and CROs are left with a fragmented ecosystem of software, hardware, […]