1. The EDE shall issue a decision to temporarily suspend the License of Medical Product Factories and Contracting Companies Manufacture Medical Products, in any of the following cases: a. Transfer of Ownership of the Factory or the Contracting Company to another person without the approval of the EDE. b. Move the Factory or the Contracting Company from the licensed location before obtaining the EDE approval. c. The absence of qualified persons for direct supervision and control in accordance with the rules in force in this field. d. Proof that the Factory or the Contracting Company used forged documents and papers while practicing their licensed activities. e. Committing the prohibitions mentioned in Clauses (4) of Article (130) of this Decree-Law. f. Any other cases that require suspension of the license of the Factory or Contracting Company as determined by the Executive Regulations of this Decree-Law. 2. The EDE shall issue an immediate decision to close the Medical Product Factories and Contracting Companies Manufacture Medical Products as precaution if continuing its operation poses a threat to public health or as a result of committing violations requiring precautionary closure as determined by the Executive Regulations of this Decree-Law. 3. In all cases, the matter must be referred to the EDE Pharmaceutical Practices Control Committee within (7) seven working days from the date of the Temporary License Suspension or Precautionary Closure to consider it and decide on disciplinary responsibility, within a period not exceeding (10) ten working days from the date refer the matter to it.
Interpretation and application must be checked against the official text and current version.