Learn more about how we are using AI technology to enhance research compliance! 

Empowering Participation

Learn about your role as a research participant, your rights and the importance of your contribution to advancing knowledge. 

Informed Consent Process is an important interactive process you will have with the study team representative about your participation in the research. Understand the critical process of informed consent and how it ensures transparency and ethical treatment in research studies. 

Are you in the stages of building an HRPP or Want to give yours a tune-up? Contact us for a free consultation. 

Explore the solution oriented services offered by our research consultants, providing expertise to researchers, sponsors, and institutions to enhance the ethical standards of research. 

What's an IRB?

Back in the mid-1900s, people got worried about some research going on that wasn't playing by the rules and wasn't treating folks in studies properly. So, they came up with these things called Institutional Review Boards (IRBs). These boards are like the guardians of ethical research—they check out studies with human participants to make sure everyone's treated fairly and kept safe. The whole idea took off, especially after a not-so-great study called the Tuskegee Syphilis Study. Nowadays, IRBs are like the superheroes of research ethics, making sure studies are done the right way.