A licensee or registrant shall: Respect and maintain the privacy and confidentiality of the client; Disclose the client's record or information about the client only with the client's consent or as required by law; Adequately safeguard confidential client information, including storage and disposal of records; Provide sufficient information to a client to allow the client to make an informed decision regarding treatment, including: The purpose or nature of an evaluation or treatment regimen; Alternatives to treatment; Side effects and benefits of a proposed treatment regimen and the alternatives to that treatment; The estimated cost of treatment and alternatives to treatment; The right of the client to withdraw from treatment at any time, including the risks associated with withdrawing from treatment; and 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; 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; Comply with applicable federal and State laws for human research programs; and Comply with applicable provisions of Health-General Article, Title 4, Subtitle 3, Annotated Code of Maryland.