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1MEDICINES AND RELATED SUBSTANCES CONTROL ACT 101 OF 1965 NOTE: The whole of this Act, except sections 1, 15B, 18, 22B, 24, 34A and 40, has been repealed by section 50 of the South African Medicines
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Medicines and related substances refer to drugs, pharmaceutical products, and any other substances used for medical purposes.
The manufacturers, distributors, and importers of medicines and related substances are required to file the relevant documentation.
The specific process and forms for filling out medicines and related substances may vary based on jurisdiction. It is important to consult the designated regulatory authority for guidance on the appropriate procedures.
The purpose of medicines and related substances is to ensure the safety, effectiveness, and quality of healthcare products, as well as to regulate their importation, distribution, and use.
The required information for reporting medicines and related substances may include product details, manufacturing processes, ingredients, packaging information, safety data, and any additional regulatory documentation.
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