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Understanding roadblocks to study activation and what your organization can do to mitigate them can ease study startup burdens.

In order to gauge the general perception and understanding of clinical research, we conducted a poll on awareness & participation in trials.

Understanding the factors that influence the decision to participate in a study helps research professionals diagnose enrollment problems.

Learn more about patient recruitment and enrollment: how they find out about clinical trials and the reasons they participate.

View this infographic to learn when do you need an endpoint adjudication committee (EAC) and what types of studies an EAC reviews.

Canadian medical device regulations can be tricky to navigate. View this infographic to learn the REB review process for medical devices.

In this infographic, we share useful information for investigators to know which level of IRB review likely applies to their study.

Tracking your research program's operational performance has many benefits. View this infographic for metrics to answer key questions.

November 3, 2021

When SARS-CoV-2 (the virus causing the disease COVID-19) broke out in 2020, the clinical research community needed to pivot quickly...

View our infographic to learn the basics of a data monitoring committee (DMC), also referred to as data safety monitoring board (DSMB).

Speed the review process by understanding how medical devices are classified & what the IRB must review to approve device research.

While the study activation process is necessary for all sites to conduct, efficiently coordinating all necessary aspects can be challenging.