Distrust triggers emotional reactions: While trust impacts hiring intentions, distrust plays a stronger role in feelings of ...

During the review process issues such as the need for local language consent forms and letters for ... it was impossible to obtain US IRB approval. This study reflects the expressed opinions and ...

The following are sample forms (consent, assent, etc.) which will need to be modified appropriately for your study and attached to your IRB submission in InfoEd. The use of these templates is not ...

ALL sections of this consent form must be completed for consideration and/or final IRB approval. If you are requesting a waiver of the standard written consent requirement, please use these templates: ...

Investigators should be aware that studies that meet the definition of clinical trial may be subject to additional regulatory and/or policy requirements, such as posting of consent forms on federal ..

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 ...

The study was reviewed by an independent IRB and followed good clinical practice and ethical principles that have their origin in the Declaration of Helsinki; all patients provided informed consent ..

This retrospective study approved by the French Ethical Committee for Research in Anaesthesia and Critical Care (IRB 00010254-2023-069 ... First, we included multiple forms of PH. Including only ...

Purpose: To develop a method to reconstruct quantitative susceptibility mapping (QSM) from multi-echo, multi-flip angle data collected using strategically acquired gradient echo (STAGE) imaging.

images along with tissue and blood samples) are predictors of treatment success. Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns.