№ lp_2_1_24712
Clinical research template issued by the National Center for Complementary and Integrative Health outlining required elements, approval conditions, monitoring procedures, and reporting expectations for study accrual and retention in funded human subjects research.
Document Type: Clinical research template and summary sheet
Title: Study Accrual and Retention Plan (SARP) Template
Version: 1.0
Date: 05Jan 2016
Organization: National Center for Complementary and Integrative Health
Acronym: NCCIH
Audience: Principal Investigators and Study Staff
Subject: Study accrual and retention planning for clinical research
Related Policy: NCCIH Policy on Study Accrual and Retention
Required Signatories: Principal Investigator; Authorizing Business Official
Submission Requirement: Approval required prior to involvement of human subjects
Reporting Frequency: At least every 4 months during enrollment and data collection
Funding Context: NCCIH-funded clinical research studies
Price: 8 / 10 USD
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