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Hospitals should access this website for a list of additional section 5506 guidelines for the policy and procedures for applying for slots, and the redistribution of the slots under sections 1886(h)(4)(H)(vi) and 1886(d)(5)(B)(v) of the Act

FDA Status and Ongoing Research Sermorelin had FDA-approved injection products in the 1990s for pediatric growth hormone deficiency and for evaluating GH secretion, but the manufacturer discontinued them and FDA withdrew the NDAs in 2009

When reporting eCQMs under the REHQR Program, REHs must adhere to the following requirements: (1) REHs must utilize technology certified to the Office of the National Coordinator for Health Information Technology's (ONC's) health information technology (IT) certification criteria, as adopted and updated in 45 CFR 170.315, for reporting eCQMs under the REHQR Program