Chapter 438 — Laboratories; Anatomical Material
ORS 438.720 Rules; inspection of organization premises and records
The Oregon Health Authority may:
In lieu of conducting inspections authorized under paragraph (b) of this subsection, accept accreditation from an accrediting body approved by the authority.
To be approved under subsection (1)(c) of this section, an accrediting body must:
Require a nontransplant anatomical research recovery organization to document processes related to the recovery, handling and distribution of anatomical material and submit to the accrediting body that documentation.
Require a nontransplant anatomical research recovery organization to keep and maintain all records related to the recovery or distribution of anatomical material for at least 10 years.
Conduct, or have a designee conduct, regular on-site compliance inspections of a nontransplant anatomical research recovery organization’s records, processes and materials relating to:
Donor intake;
Acquisition, preparation, labeling, packaging, storage and distribution of anatomical material; and
Any inspection of a facility owned or operated by the nontransplant anatomical research recovery organization.
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Provenance
2023 Oregon Revised Statutes
Official online edition
- Source
- oregonlegislature.gov
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Version history
Prior statutory text is not available in the ingested published editions. Consult an earlier official ORS edition or the cited Oregon Laws chapter.
2025 Oregon Revised Statutes — official online source · active · operative text
Official source2023 Oregon Revised Statutes · active · operative text
Official source