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… data, these technologies require the guidance of content experts to ensure they are applied appropriately. …
… Collection Request (ICR) for IPAY 2027, with a 60-day public comment period. The ICR will describe how CMS will … Be part of the process, be ready for what is coming, and understand whether you have the capacity to … among other considerations This deadline is the day after CMS publishes an explanation of Round 1 …
… is our calling, and we are committed to living it every day, in our work and in our actions,” said RTI President and …
Using RTI Rarity™ to Support Clinical Trial Diversity Requirements Local Social Inequity Score Offers Precise Analysis of Social Risk Data The US Food and Drug Administration (FDA) recently released guidance that outlines specific diversity requirements …
Discovering What Treatment Options are Most Important to Patients With Psoriatic Arthritis Share on: June 29, 2022 Despite recent advances in the treatment of psoriatic arthritis (PsA), for some who live with the condition, available treatments do not …
… though, most patients experience periods during the day of "OFF" episodes (worsening of symptoms), even when …
… development, and resource allocation. She supports the day-to-day functions of project teams and has managed large, complex … and quality review processes. In addition to her day-to-day project-focused responsibilities, Ms. Siersma …
Advancing Health Equity: The Crucial Role of Pharma and Medtech Developers Share on: November 14, 2023 Image Contributor: Mark Price, MEd, MA Head, Economic QUalitative Inquiry, Policy, and Access RTI Health Solutions This is part two of a three-part …
Real-World Evidence Fills Gaps in Blood Cancer Research Share on: February 12, 2022 Most of what we know about treatments, adverse events, and the overall survival of patients with chronic lymphocytic leukemia (CLL) and mantle cell lymphoma (MCL) comes …
… as a communication and collaboration tool for exchanging content, and no regulatory decisions may be made directly … The authoritative source document(s) for all regulatory content must remain within the respective party’s validated … You must notify RTI-HS within one (1) business day if a person you have authorized for access to the SPO …