Univo IRB

We are delighted to bring additional industry experienced employees to the growing Univo team. Please welcome Victoria Haggett and Kelly Shaffer, MS. Scaling a business requires bringing in top talent such as these two. We invest in our employees and culture which is proving to have a great impact on our customer service. Here's a few of the areas that these two bring to the team: CRO, global study start-up, neurology, cardiology, endocrinology, dermatology, oncology, hematology, ophthalmology, psychology, informed consent development, regulatory submissions, regulatory compliance, clinical research finance, medical terminology, phase I-III, research assistant at hospitals and institutions.

Ever wonder what the cost of a day delay in #clinicaresearch is? TUFTS shares insightful data in this latest report. Reach out to learn how our high-touch service helps you meet timelines and navigate this changing industry. https://ow.ly/uvcB50SQ7fH

The metrics are in, and Univo's new IRB submission platform is exceeding our expectations. Take a look at these numbers. If this is not your experience, we can change that for you.

Society for Clinical Research Sites (SCRS) is all about reshaping the way we approach research – sound familiar? Schedule time with Julie Blasingim, Bailey Sterrett, Diane Maragos, and Matt Ullum, at Booth #623 to talk about how our unique IRB approach can revolutionize your trial. https://lnkd.in/gvp6bsmG    #SCRS #IRB #clinicaltrials

IRBs should be focused on protecting patients, not trying patience. That’s exactly what we do. See how on our website, and keep an eye out for a special announcement coming soon! https://ow.ly/oYq850SQ6Py #patientcentricity #IRB #patientsaftey

Get to study start up faster by meeting Univo IRB at #DPHARM! Matt Ullum and Bailey Sterrett will be at Booth #12 – book time with them now to learn how our agile customer service, industry-leading technology, and commitment to patient advocacy can help your trial. https://lnkd.in/gJYXixWP  #patientadvocacy #clinicaltrials 

OneVerse™, our propriety IRB platform, ensures a simplified review process so you can get to study start up faster. Explore its features or request a demo here: https://lnkd.in/gBGNcfaq #IRB #OneVerse #clinicaltrials

What does FDA's Diversity Action Plans mean and how do you plan to use them. Here's a quick summary of the FDA Guidance and what is can mean for you.

Meet Julie Blasingim, a seasoned IRB executive with 20 years of regulatory, operational, and compliance experience in human research protection and site operations.     Why is she passionate about unifying patients and research? “We are all patients at some point. We need to see less people suffer from diseases that take them too soon. We want our kids to have better healthcare options.”    Want to put Julie’s expertise to work for your study? Visit our website now! https://lnkd.in/gigTRD_e   #IRB #clinicaltrials #TeamUnivo   

As the data in this report shows, we will not bridge research and patients until we improve research access. What remote research solutions have you tried to bring your trial to more patients? Did they work? Share in the comments. https://ow.ly/ZPeQ50SQ57y  #clinicaltrials #patientcentric #DCTs