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The 2010 Guidance states that following it is voluntary, though many of its specific recommendations serve to remind providers of their obligations under existing regulations. Copy claim link
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Supporting evidence: primary · 1 source
Provision Standing · provision ID us-hhs-screening-guidance-2010-voluntary-standing Subject version As published in the Federal Register of 13 October 2010 (75 FR 62820) · Published 2010-10-13 · Effective 2010-10-13 Date 2010-10-13 · publication Scope and limits The notice's statement about its own standing, not a finding about any provider's practice; the existing regulations it refers to are not recorded here. Split under the one-claim-per-edge rule from the record that also carried the Guidance's addressees, which are now the separate record recorded separately. The provision kind is the nearest the dataset schema admits (the schema has no kind for an instrument's standing): the sentence states that the Guidance itself imposes no duty beyond obligations existing regulations already carry. See openQuestions. The provision kind is now `standing` (schema 2.22), the kind for the standing a text claims for itself, where part 1 used `exception`.
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Screening Framework Guidance for Providers of Synthetic Double-Stranded DNA (75 FR 62820) ↗ Federal Register (Office of the Federal Register, National Archives) via govinfo.gov · Publication date unknown
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Source excerpt “Following this Guidance is voluntary, though many specific recommendations serve to remind providers of their obligations under existing regulations.” Location in source SUMMARY, 75 FR 62820
How it was read Retrieved directly from the publisher
Machine-checked · 2026-10-30
Source details and check notes Authors Federal Register (Office of the Federal Register, National Archives) via govinfo.gov Version Retrieved for the candidate pack on 2026-10-28 (SHA-256 d3bfd95a1e3ae4d212505081166f0f8bb7475845e225ae643e6d4a03a93b7e56). Federal Register print of 13 October 2010, Vol. 75, No. 197, pp. 62820-62832, FR Doc. 2010-25728. The notice publishes the final Guidance in full, after the comment responses. Retrieved again at admission on 2026-10-30 (SHA-256 d3bfd95a1e3ae4d212505081166f0f8bb7475845e225ae643e6d4a03a93b7e56, the same bytes). Canonical address Open the canonical source ↗ Accessed 2026-10-28 Language English (en) Attribution Federal Register (Office of the Federal Register, National Archives) via govinfo.gov, “Screening Framework Guidance for Providers of Synthetic Double-Stranded DNA (75 FR 62820)”. Reuse No open redistribution licence asserted. Bibliographic metadata, editorial paraphrases and short attributed quotations (at most 50 words each). Recheck terms before wider redistribution. Check notes Candidate pack passage, AI and biosecurity (research/ai-bio). The quotation (19 words) matched the text retrieved for the candidate pack on 2026-10-28 and again at admission on 2026-10-30, in a fresh retrieval whose SHA-256 equals the pack’s. Matching ignored differences of whitespace, case, quotation marks, dashes and Unicode compatibility forms, so the source’s typography can differ. No human editorial review. Status and meaning Editorial status. Not reviewed by an editor . An exploratory record that no editor has accepted. This status does not say whether a person has read any linked passage. Each evidence record above shows how it was checked.
Relation. An exact framework edition, or another document with an exact expression, states one provision: a capability threshold or risk level and its trigger, a required safeguard or action, a decision authority (who decides, recommends, can overrule or is informed), a stated exception, or another statement of its content, such as a licence term or a prospectus statement. The passage records what the document says, not implementation, compliance or effectiveness. Provisions with the same key align across editions of one family.
Date. Provision as the 2010 expression states it, dated by its publication in the Federal Register of 13 October 2010.
Record ID ab-scr-hhs-2010-voluntary-all-providers