Section 318:51-b – Licensing of Limited Retail Drug Distributors Required.
318:51-b Licensing of Limited Retail Drug Distributors Required. – I. No person shall operate as a limited retail drug distributor, as defined in RSA 318:1, VII-a, without first having obtained a license to do so from the board. Such license shall expire biennially on June 30 of each odd-numbered year. An application together with […]
Section 318:51-c – Licensing of Outsourcing Facilities Identified as Section 503B Facilities by the United States Food and Drug Administration.
318:51-c Licensing of Outsourcing Facilities Identified as Section 503B Facilities by the United States Food and Drug Administration. – I. No person shall compound legend drugs or controlled drugs, as defined in RSA 318-B:1, VI, and no person acting as or employed by an outsourcing facility shall supply such drugs, without first having obtained […]
Section 318:51-d – Repealed by 2015, 180:4, eff. July 22, 2017.
318:51-d Repealed by 2015, 180:4, eff. July 22, 2017. –
Section 318:51-e – Rulemaking.
318:51-e Rulemaking. – The board shall adopt rules pursuant to RSA 541-A relative to: I. [Repealed.] II. Content of the application; III. The standards for licensing of outsourcing facilities; IV. [Repealed.] V. Standards for denial and revocation of license; VI. Inspection requirements; VII. Dispensing and distribution requirements of prescription drugs; VIII. Record keeping requirements; […]
Section 318:51-f – Licensure of Research Organizations.
318:51-f Licensure of Research Organizations. – I. No research organization shall procure or conduct research operations with prescription drugs by researchers without first having obtained a license from the board. Such license shall expire biennially on June 30 of each odd-numbered year. An application together with a reasonable fee as established by the board […]
Section 318:51-g – Licensure of Drug or Device Distribution Agents.
318:51-g Licensure of Drug or Device Distribution Agents. – I. No person shall act as a prescription drug or device distribution agent, which includes controlled drugs as the term is defined in RSA 318-B:1, VI, without first having obtained a license to do so from the board. II. Any person licensed pursuant to this […]
Section 318:52 – Repealed by 1971, 135:2, eff. July 20, 1971.
318:52 Repealed by 1971, 135:2, eff. July 20, 1971. –
Section 318:52-a – Fraud or Deceit.
318:52-a Fraud or Deceit. – It is unlawful to obtain or attempt to obtain a drug or device sold by prescription of a physician, dentist, optometrist, podiatrist, veterinarian, naturopathic doctor, physician assistant, or advanced practice registered nurse that bears a statement that it is to be dispensed or sold only by or on the […]
Section 318:52-b – Destruction of Used Instruments in Health Care Facilities.
318:52-b Destruction of Used Instruments in Health Care Facilities. – It shall be unlawful for any possessor of a hypodermic syringe, needle, or any instrument adapted for the administration of controlled drugs, in health care facilities, to dispose of or discard any such instrument in any manner other than that provided in this section. […]
Section 318:47-l – Hormonal Contraceptives; Dispensing.
318:47-l Hormonal Contraceptives; Dispensing. – I. In this section, " standing order " means a written and signed protocol authored by one or more physicians licensed under RSA 329:12 or one or more advanced practice registered nurses licensed under RSA 326-B:18. Such agreement shall specify a protocol allowing the pharmacist licensed under RSA 318:18 […]