Title 16, TITLE 16. HEALTH

"bedroom equivalent" Sec. 0.4. (a) As used in this chapter, "residential onsite sewage system" means all equipment and devices necessary for proper conduction, collection, storage, treatment, and onsite disposal of sewage from: (1) a one (1) or two (2) family dwelling; (2) a resi…

for residential onsite sewage system; installation of residential onsite sewage system in fill soil in certain counties Sec. 1. (a) The state department shall adopt rules under IC 4-22-2 that provide for a reasonable period not exceeding thirty (30) days in which a plan review an…

sewage system is located for inspection Sec. 10. (a) Neither an officer or employee of a local health department nor another agency, officer, or employee of a county, city, or town may enter property on which a residential onsite sewage system is located for the purpose of inspec…

department order to correct residential onsite sewage system failure; private inspection to determine system status Sec. 11. (a) As used in this section, "residential onsite sewage system failure" means a residential onsite sewage system that exhibits one (1) or more of the follo…

Sec. 12. (a) As used in this section, "onsite sewage system service" means: (1) installing; (2) inspecting; and (3) providing maintenance and repair services for; residential onsite sewage systems. (b) An individual who: (1) is registered with at least one (1) county in Indiana t…

Sec. 2. (a) Except as otherwise provided, a person who recklessly violates or fails to comply with rules adopted under section 1 of this chapter commits a Class B misdemeanor. (b) Each day a violation continues constitutes a separate offense. [Pre-1993 Recodification Citation: 16…

requirements; violation; enforcement Sec. 3. (a) This section applies only to residential onsite sewage systems that are installed after July 1, 1996, and that use a raiser that is more than six (6) inches in diameter and opens to ground level. (b) Each opening to an underground …

to whether property located in regional sewer district; qualifications for local health department employee to conduct onsite soil evaluation Sec. 4. (a) Before a local health department may act on an application for a residential onsite sewage system permit, the local health dep…

department's rule; certification of professional engineer concerning planned or existing residential onsite sewage system Sec. 5. (a) The authority of a local health department to administer the rule of the state department concerning residential onsite sewage systems is subject …

in compacted soil; certification of registered soil scientist as to suitability; denial of permit prohibited Sec. 6. A local health department may not deny a permit for the construction or installation of a residential onsite sewage system in a particular location on the grounds …

for residential onsite sewage systems; more stringent requirements than those of state department's rule prohibited after June 30, 2023 Sec. 7. (a) After June 30, 2023, a county, city, or town ordinance may not adopt requirements, restrictions, or conditions concerning the: (1) d…

Sec. 7.2. (a) As used in this section, "sinkhole" means a depression or hole in the ground caused by some form of collapse of the surface layer, as when subsurface limestone is dissolved or worn away by the movement of water underground. (b) A residential onsite sewage system sha…

health department or certain professionals; permit to be issued within 30 days of receipt of complete application; authority of local health department to inspect system Sec. 8. (a) If: (1) an application has been filed with a local health department for a permit for the installa…

Sec. 8.5. (a) As used in this section, "lot" means the parcel of real property on which: (1) a one (1) family or two (2) family dwelling; or (2) two (2) single family dwellings located on the same property with a combined design daily flow of not more than seven hundred fifty (75…

permit required; reports to department Sec. 9. (a) As used in this section, "septage" means human excreta, wastewater, scum, sludge, and other content introduced through incidental or accidental seepage that is removed from domestic septic tanks, holding tanks, privies, seepage p…

Sec. 1. As used in this chapter, "biological product" means: (1) a virus; (2) a therapeutic serum; (3) a toxin; (4) an antitoxin; (5) a vaccine; (6) blood; (7) a blood component; (8) a blood derivative; (9) an allergenic product; (10) a protein (except any chemically synthesized …

Sec. 2. As used in this chapter, "biosimilar" refers to a biological product that: (1) has been licensed as a biosimilar product under 41 U.S.C. 262(k) or has been approved based on an application filed under 21 U.S.C. 355(b)(2); and (2) is highly similar to the reference product…

Sec. 3. As used in this chapter, "interchangeable" means: (1) a determination by the federal Food and Drug Administration that a biosimilar product may be substituted for a reference biological product without the intervention of the health care provider that prescribed the biolo…

Sec. 4. A pharmacist may substitute for a prescribed biological product if the following conditions are met: (1) The substitute has been determined by the federal Food and Drug Administration to be interchangeable with the prescribed biological product. (2) The prescribing practi…

Sec. 5. (a) Except as provided in subsection (b), in order to ensure medical records are complete and accurate, a pharmacist shall, not later than ten (10) calendar days after dispensing a biologic product, record the name and manufacturer of the biologic product dispensed using:…

Sec. 6. (a) The pharmacy shall retain a record in accordance with IC 25-26-13-25(a) of the dispensed biological product. (b) The prescribing practitioner shall retain a record in accordance with IC 16-39-7-1 of the dispensed biological product. As added by P.L.96-2014, SEC.6.

rules Sec. 7. (a) The Indiana board of pharmacy shall maintain a link on the board's Internet web site to the current list of all biological products determined by the United States Food and Drug Administration to be interchangeable with a specific reference biological product. (…

Sec. 8. A written or electronic prescription for a biological product must comply with the requirements under IC 16-42-22-6. As added by P.L.96-2014, SEC.6.