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Direct Entry Midwifery Legend Drugs and Devices Proposed Rules Comments Due April 30

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Summary

The Oregon Health Authority Health Licensing Office and Board of Direct Entry Midwifery have filed proposed administrative rules governing legend drugs and devices for direct entry midwives. The proposed rules require applicants to pass a written examination plus three skills examinations covering injection administration, intravenous therapy, and suturing before licensure. Currently licensed direct entry midwives must retake both the written and skills assessment examinations every three years for license renewal. Comments will be accepted through April 30 2026 at noon with a public hearing scheduled for April 29 2026 from 10 a.m. to noon. Permanent rules are scheduled to become effective July 1 2026.

“Comments will not be accepted or considered if received after 12 p.m. (noon) on April 30, 2026.”

OHA HLO , verbatim from source
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GovPing monitors OR Healthcare Regulation & Quality Improvement for new healthcare & life sciences regulatory changes. Every update since tracking began is archived, classified, and available as free RSS or email alerts — 2 changes logged to date.

What changed

The proposed rules establish examination requirements for direct entry midwives who purchase and administer authorized scheduled legend drugs and devices for pregnancy, birth, postpartum, and newborn care. New applicants must pass a written exam plus three skills exams covering injection, IV therapy, and suturing to demonstrate baseline competency. Currently licensed midwives will be required to retake both the written and skills examinations every three years upon license renewal. The rules are being refiled in the April 2026 Oregon Bulletin to incorporate additional fiscal impact details and hearing information. Comments are open through April 30 2026 with a public hearing on April 29 2026.

Affected parties include licensed direct entry midwives in Oregon who must budget for recurring examination requirements and new applicants preparing for the comprehensive assessment process. Midwives should review the proposed rule text and consider submitting comments on the competency standards, examination requirements, and three-year renewal cycle before the comment deadline.

Hearing

Date
2026-04-29 at 10:00 – 12:00
Location
Hybrid

Archived snapshot

Apr 22, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

HLO News Details

Proposed Rules: Direct Entry Midwifery Legend Drugs & Devices

Wednesday, April 1, 2026

The Oregon Health Authority, Health Licensing Office (HLO), and the Board of Direct Entry Midwifery (Board) are notifying interested parties that proposed administrative rules have been filed with the Secretary of State's Office for publication in the April 2026 Oregon Bulletin.

The Notice of Proposed Rulemaking includes the possible fiscal impacts, a racial equity statement, and the proposed rule text. Permanent administrative rules are scheduled to become effective on July 1, 2026.

The documents linked below include:

Notice of Proposed Rulemaking: Secretary of State version

DEM Proposed Rules – bold and strikethrough version

​A Notice of Proposed Rulemaking for legend drugs and devices was filed and published in the March 2026 Oregon Bulletin. The Notice of Proposed Rulemaking is being refiled and republished in the April 2026 Oregon Bulletin to incorporate additional fiscal impact details and hearing information.

Need for Rules: Summary Licensed direct entry midwives have the authority to purchase and administer authorized scheduled legend drugs and devices for use in pregnancy, birth, postpartum care, and newborn care if deemed integral to providing safe care to birthing persons and newborns.

These rules require applicants to pass an examination consisting of a written exam and three skills exams related to legend drugs and devices. The three skills exams include administration of medication through injection, intravenous therapy, and suturing, ensuring that applicants can demonstrate and meet baseline competency in each skill area prior to licensure.

These rules also require currently licensed direct entry midwives to retake the legend drugs and devices written and skills assessment examinations every three years in order to renew their licenses.

You are invited to review the proposed rules and submit comments from March 1 to April 30, 2026, until 12 p.m. (noon). Comments may be submitted to Josh Page at josh.page@oha.oregon.gov or by mail to:

Attn: Josh Page
Health Licensing Office
1430 Tandem Ave. NE, Suite 180
Salem, OR 97301-2192

A public rule hearing has been scheduled for April 29, 2026, from 10 a.m. to 12 p.m. (noon). Interested parties may attend the hearing in person at the address listed above or via Zoom.

| Ways to attend: | How to attend the meeting:

(If not attending in person, follow one of the options below) | ​ | ​ |
| ​ | Join By: | **** Meeting or Conference ID: | Passcode: |
| Zoom Video (audio/video) | Join the meeting now | Meeting ID: 161 553 9814 | 819789 |
| Zoom Audio

(audio only) | Dial (669) 254-5252 | Meeting ID: 161 553 9814 | |

Instructions for attending via Zoom:

  • Email your full name to Samie Patnode at samie.patnode@oha.oregon.gov and state that you would like to testify.
  • The HLO asks that individuals attending the hearing via Zoom keep their cameras off and their phones or microphones muted during the entire hearing, until their name is called to testify. Comments will not be accepted or considered if received after 12 p.m. (noon) on April 30, 2026. For more information or to request this information in an alternative format, please call Josh Page at (503) 934-0720 or email josh.page@oha.oregon.gov.

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Named provisions

Legend Drugs and Devices Examination Requirements License Renewal Assessment Standards

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Last updated

Classification

Agency
OHA HLO
Published
April 1st, 2026
Comment period closes
April 30th, 2026 (7 days)
Instrument
Consultation
Branch
Executive
Legal weight
Non-binding
Stage
Consultation
Change scope
Substantive

Who this affects

Applies to
Healthcare providers
Industry sector
6211 Healthcare Providers
Activity scope
Licensure examination Drug administration authority Healthcare credentialing
Geographic scope
US-OR US-OR

Taxonomy

Primary area
Healthcare
Operational domain
Compliance
Topics
Pharmaceuticals Medical Devices

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