Current through Register Vol. 51, No. 22, November 1, 2024
Section 10.65.03.06 - Records, Confidentiality, and Informed ConsentA licensee or registrant shall:
A. Respect and maintain the privacy and confidentiality of the client;B. Disclose the client's record or information about the client only with the client's consent or as required by law;C. Adequately safeguard confidential client information, including storage and disposal of records;D. Provide sufficient information to a client to allow the client to make an informed decision regarding treatment, including: (1) The purpose or nature of an evaluation or treatment regimen;(2) Alternatives to treatment;(3) Side effects and benefits of a proposed treatment regimen and the alternatives to that treatment;(4) The estimated cost of treatment and alternatives to treatment;(5) The right of the client to withdraw from treatment at any time, including the risks associated with withdrawing from treatment; and(6) The client's right to decline to participate in treatment if an aspect of the treatment will be recorded, documented, photographed, observed, or otherwise used in an educational program;E. Obtain the full informed consent of a client participating in a human research program, without a direct or implied penalty for the client's refusal to participate in the program, and with due regard for the client's autonomy and dignity;F. Comply with applicable federal and State laws for human research programs; andG. Comply with applicable provisions of Health-General Article, Title 4, Subtitle 3, Annotated Code of Maryland.Md. Code Regs. 10.65.03.06
Regulations .06 recodified from .06 effective 43:26 Md. R. 1446, eff. 1/2/2017; amended effective 51:15 Md. R. 710, eff. 8/5/2024.