1. No person, who has knowledge by virtue of his or her office of the identity of a particular patient or research subject, a manufacturing process, a trade secret or a formula shall disclose such knowledge, or any report or record thereof, except: (a) to another person employed by the department, for purposes of executing provisions of this article; (b) pursuant to judicial subpoena or court order in a criminal investigation or proceeding; (c) to an agency, department of government, or official
ORS 431.966 Amended by 2015 Ch. 736, § 74, eff. 7/20/2015, op. 1/1/2016. Amended by 2013 Ch. 550, § 4, eff. 1/1/2014. 2009 c. 799, § 4; 2011 c. 720, § 186
(a) Prescription monitoring data: (1) Are confidential and privileged, and not subject to discovery, subpoena, or other means of legal compulsion in civil litigation; (2) Are not public records; and (3) Except as provided in subsections (b), (c), (d), and (f) of this section or as otherwise provided by law, may not be disclosed to any person. (b) The Program shall disclose prescription monitoring data, in accordance with regulations adopted by the Secretary, to: (1) A prescriber, or a licensed health
(a) The controlled substance prescription database is established in the Board of Pharmacy. The purpose of the database is to contain data as described in this section regarding every prescription for a schedule II, III, or IV controlled substance under federal law dispensed in the state to a person other than under the circumstances described in (u) of this section. (b) The pharmacist-in-charge of each licensed or registered pharmacy, regarding each schedule II, III, or IV controlled substance under
(a) Except as otherwise provided in subsections (c), (c.1), and (d) of this Code section, prescription information submitted pursuant to Code Section 16-13-59 shall be confidential and shall not be subject to open records requirements as contained in Article 4 of Chapter 18 of Title 50. (b) The department, in conjunction with the board, shall establish and maintain strict procedures to ensure that the privacy and confidentiality of patients, prescribers, and patient and prescriber information collected
Subdivision 1.Definitions. (a) For purposes of this section, the terms defined in this subdivision have the meanings given. (b) "Board" means the Minnesota State Board of Pharmacy established under chapter 151. (c) "Controlled substances" means those substances listed in section 152.02, subdivisions 3 to 6, and those substances defined by the board pursuant to section 152.02, subdivisions 7, 8, and 12. For the purposes of this section, controlled substances includes butalbital and gabapentin. (d)
(a)Standard: notice of privacy practices - (1)Right to notice. Except as provided by paragraph (a)(2) or (3) of this section, an individual has a right to adequate notice of the uses and disclosures of protected health information that may be made by the covered entity, and of the individual's rights and the covered entity's legal duties with respect to protected health information. (2)Exception for group health plans. (i) An individual enrolled in a group health plan has a right to notice: (A) From