Md. Code, Commercial Law § 14-4802
This is the official text of Md. Code, Commercial Law § 14-4802, part of Maryland’s Code, Commercial Law — governs commercial transactions - Maryland's version of the Uniform Commercial Code.
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§14–4802.
Official statutory text
This subtitle does not apply to:
(1) Data subject to a statute or regulation identified under item (i) of this item that is controlled by a covered entity or service provider that is:
(i) Required to comply with:
1. Title V of the federal Gramm–Leach–Bliley Act;
2. The federal Health Information Technology for Economic and Clinical Health Act; or
3. Regulations promulgated under § 264(c) of the Health Insurance Portability and Accountability Act of 1996; and
(ii) In compliance with the information security requirements of applicable statutes or regulations identified in item (i) of this item; or
(2) Information collected as part of a clinical trial subject to the Federal Policy for the Protection of Human Subjects, in accordance with:
(i) Good clinical practice guidelines issued by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use; or
(ii) Human subject protection requirements of the U.S. Food and Drug Administration.
(1) Data subject to a statute or regulation identified under item (i) of this item that is controlled by a covered entity or service provider that is:
(i) Required to comply with:
1. Title V of the federal Gramm–Leach–Bliley Act;
2. The federal Health Information Technology for Economic and Clinical Health Act; or
3. Regulations promulgated under § 264(c) of the Health Insurance Portability and Accountability Act of 1996; and
(ii) In compliance with the information security requirements of applicable statutes or regulations identified in item (i) of this item; or
(2) Information collected as part of a clinical trial subject to the Federal Policy for the Protection of Human Subjects, in accordance with:
(i) Good clinical practice guidelines issued by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use; or
(ii) Human subject protection requirements of the U.S. Food and Drug Administration.
Status: in_force · Read it on the official government site
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