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37 PHARMACY EXAMINING BOARD Par 18.03 Chapter Par 18 PRESCRIPTION DRUG MONITORING PROGRAM Par 18.01 Par 18.02 Par 18.03 Par 18.04 Par 18.05 Par 18.06 Par 18.07 Authority and scope. Definitions. Drugs
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What is chapter phar 18?
Chapter phar 18 is a section of pharmaceutical regulations governing the manufacturing and distribution of drugs.
Who is required to file chapter phar 18?
Manufacturers and distributors of pharmaceutical products are required to file chapter phar 18.
How to fill out chapter phar 18?
Chapter phar 18 must be filled out according to the specific requirements outlined in the regulations.
What is the purpose of chapter phar 18?
The purpose of chapter phar 18 is to ensure the quality and safety of pharmaceutical products.
What information must be reported on chapter phar 18?
Chapter phar 18 requires information on the manufacturing process, ingredients used, and quality control measures.
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