Preliminary data indicate the treatment or diagnostic procedure or device has improved net health and functional outcomes; and
No alternative treatment or diagnostic is available; or
A controlled, clinical trial that has been reviewed and approved by an institutional review board that was established in accordance with the federal Department of Health and Human Services (DHHS) regulations ( 45 C.F.R. Part 46 consistent with the purposes of this chapter, and as now or hereafter amended); and
For medical devices not yet cleared for marketing, the clinical evaluation has an approved investigational device exemption (IDE) in accordance with the federal Food and Drug Administration (FDA) regulations (21 C.F.R. Parts 50, 56, and 812 consistent with the purposes of this chapter, and as now or hereafter amended); and
For drugs not yet cleared for marketing, the clinical evaluation has been approved in accordance with the federal Food and Drug Administration (FDA) regulations ( 21 C.F.R. Part 312 consistent with the purposes of this chapter, and as now or hereafter amended); or
Wash. Admin. Code § 296-20-02850
Statutory Authority: RCW 51.04.020 and 51.04.030. 00-01-037, § 296-20-02850, filed 12/7/99, effective 1/8/00.