1. The Competent Health Establishment or Authority, each within the limits of their jurisdiction, shall issue a decision to cancel the approval issued by it for the safe disposal or destruction of the Medical Product and inform the Entity referred to in paragraph (c) of Clause (1) of Article (49) of this Decree-Law of that, in any of the following cases: a. If it is proven that obtaining approval was a result of submitting forged documents or incorrect information. b. The absence of any of the conditions for issuing approval to advertise the Medical Product mentioned in Clause (1) of Article (49) of this Decree-Law, after publishing the advertisement. c. Any other cases determined by the Executive Regulation of this Decree-Law. 2. The Ownership of the approval for safe disposal or destruction of the Medical Product may not be transferred to another party, and a new application for approval for safe disposal or destruction of the Medical Product shall be submitted.
Interpretation and application must be checked against the official text and current version.