Grants and Contracts Details
HUMAN CLINICAL TRIAL - CONFIDENTIAL In accordance with the Protocol, Site will be responsible for performing the following: Obtaining local IRB approval and mailing approval letter to Principal Investigator. Recruiting and organizing Services personnel at Site. Participating in Services wide training (e.g., PowerPoint lecture, practice charts). Identifying patients hospitalized with acute asthma per Protocol. Completing an online site survey. Completing at least 40 chart reviews of patients hospitalized with acute asthma. Responding to data queries, as needed.
|Effective start/end date||12/22/14 → 11/30/15|
- Massachusetts General Hospital: $3,500.00
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