New in Concentriq for Research 3.9: Expanded Capabilities for Preclinical R&D

Join our upcoming webinar to learn about important enhancements we’ve made to Concentriq for Research to help you and your team accelerate GLP and non-regulated drug safety studies.

Preclinical R&D centers around workflows that involve massive volumes of data. We’ve expanded Concentriq for Research to help life sciences organizations increasingly realize the efficiency and quality gains that the platform delivers across the R&D value chain.

Register for this upcoming webinar for a deeper dive into how we are enabling preclinical R&D, including:

• Robust capabilities for Good Practice Practice (GLP) compliance, enabling life science organizations to conduct all of their GLP and non-regulated studies in a single digital environment.
• A new Studies module that streamlines toxicopathology workflows, including whole slide image scoring and peer review.
• An improved version of our embedded Automated Quality Control that now detects commonly occurring quality issues in ever image of H&E, IHC, and special stained slides.

Edaeni Hamid, PhD

Product Director, Proscia

Edaeni Hamid is a Senior Product Manager at Proscia. Edaeni received her PhD in Neuroscience from the University of Illinois, Chicago. She continued her work in biomedical research as a postdoctoral fellow at NIH. Prior to Proscia, she worked with Nikon and a Neurotechnology startup. She is passionate about leveraging emerging technology to enable breakthrough scientific discoveries that positively impact human health.