Md. Code Ann., Health-Gen. § 3-403
Committee on Registered Nurses Personally Preparing and Dispensing Drugs and Devices in Local Health Departments
Effective Oct 1, 2024Added by Acts 2015, c. 44, § 1, eff. June 1, 2015. Amended by Acts 2017, c. 62, § 1, eff. April 11, 2017; Acts 2024, c. 932, § 1, eff. Oct. 1, 2024; Acts 2024, c. 933, § 1, eff. Oct. 1, 2024.State of Maryland
(a)
- (1) There is a Committee on Registered Nurses Personally Preparing and Dispensing Drugs and Devices in Local Health Departments.
(2) The Committee consists of the following members:
- (i) A representative of the Department, appointed by the Department;
- (ii) A representative of the State Board of Nursing, appointed by the State Board of Nursing;
- (iii) A representative of the State Board of Pharmacy, appointed by the State Board of Pharmacy;
- (iv) A representative of the State Board of Physicians, appointed by the State Board of Physicians;
- (v) A pharmacist who practices in the State, appointed by the State Board of Pharmacy;
- (vi) A registered nurse who practices in the State, appointed by the State Board of Nursing;
- (vii) A representative of the Office of Controlled Substances Administration, appointed by the Office; and
- (viii) A representative of a local health department, appointed by the Department.
(3)
- (i) The term of a member is 4 years.
- (ii) At the end of a term, a member continues to serve until a successor is appointed.
(4) A member of the Committee:
- (i) May not receive compensation as a member of the Committee; but
- (ii) Is entitled to reimbursement for expenses under the Standard State Travel Regulations, as provided in the State budget.
- (5) The Secretary shall designate the chair of the Committee.
- (6) The Department shall provide staff for the Committee.
(b) The Committee shall:
- (1) Develop and approve a formulary for use by registered nurses that includes all nonprescription contraceptive drugs and devices approved by the U.S. Food and Drug Administration for over-the-counter use; and
- (2) Annually review the formulary to ensure compliance with current prescribing standards.
Added by Acts 2015, c. 44, § 1, eff. June 1, 2015. Amended by Acts 2017, c. 62, § 1, eff. April 11, 2017; Acts 2024, c. 932, § 1, eff. Oct. 1, 2024; Acts 2024, c. 933, § 1, eff. Oct. 1, 2024.