Information related to the IRB submission process. The UB IRB has updated the HRP-503 Template Protocol (IRB Version: JAN2016). All new studies submitted on or after April 1, 2016 must be submitted ...

and are responsible for review and approval of clinical research protocols including those where pHSC are administered to human subjects. The Institutional Animal Care and Use Committee The ...

Real world data (RWD), which is data from actual patient treatments, provides valuable information on safety and effectiveness of innovative ...

Correspondence to Dr Thomas Bandholm, Dept of Clinical Research ... more or less be copy-pasted from your protocol. During the planning and conduct of your trial, however, others may have published ...

Rua Dr. Diogo de Faria, 1087 – 9º andar – Vila Clementino 04037-003 São Paulo/SP - Brasil E-mail: scielo@scielo.org ...

As a result of these disruptions, NIH staff has reported being unable to meet with study participants or recruit patients into clinical trials, delays submitting research findings to science ...

Victorson is a professor of medical social sciences at the Northwestern University Feinberg School of Medicine. When I read the recent news that the Trump administration has frozen all federally ...

More information: Ayako Takemori et al, PEPPI-MS: gel-based sample pre-fractionation for deep top-down and middle-down proteomics, Nature Protocols (2025). DOI: 10.1038/s41596-024-01100-0 ...

The NIH is the crown jewel of American scientific research, investing most of its $47 billion budget on medical research. Without the NIH meetings known as study sections, the agency can’t revie ...