Section 21-225 – New Drugs — Inspection of Records
Any person who is required under § 21-223 or § 21-224 of this subtitle to keep records and any person who is in charge or custody of any of these records, on the request of the Secretary, shall permit the Secretary to have access to, copy, and verify the records at any reasonable time.
Section 21-226 – Printed Information for Use of Practitioners
(a) The manufacturer, packer, or distributor of any prescription drug that is sold or distributed in this State shall: (1) Keep correct copies of any printed matter that is: (i) Required to be included in any package in which the drug is sold or distributed; or (ii) Approved under the federal act; and (2) Send copies of the printed matter […]