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This document establishes the criteria and procedures for drug registration in Indonesia, focusing on the protection of public health through the evaluation of drug efficacy, safety, and quality before
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How to fill out Decree of the Head of National Agency of Drug and Food Control

01
Obtain the Decree template from the National Agency of Drug and Food Control's official website or their office.
02
Fill in the required details such as applicant's name, address, and contact information.
03
Specify the purpose of the application in the designated section.
04
Include any relevant supporting documents, such as certificates or licenses, as required.
05
Review the filled-out Decree to ensure all information is accurate and complete.
06
Submit the completed Decree to the appropriate department within the National Agency of Drug and Food Control.

Who needs Decree of the Head of National Agency of Drug and Food Control?

01
Pharmaceutical companies seeking approval for new drugs.
02
Food manufacturers wanting to register their products.
03
Healthcare providers needing authorization for specific medical equipment.
04
Individuals or organizations conducting research involving drugs or food safety.
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The Decree of the Head of National Agency of Drug and Food Control is a formal regulation or order issued by the agency to establish guidelines and standards for the regulation of drugs and food products, ensuring their safety, efficacy, and quality.
Individuals and organizations involved in the production, distribution, or marketing of food and drug products are required to file the Decree of the Head of National Agency of Drug and Food Control to comply with regulations.
To fill out the Decree of the Head of National Agency of Drug and Food Control, individuals must provide accurate information regarding the product, including its composition, intended use, manufacturing details, and compliance with safety standards.
The purpose of the Decree is to protect public health by ensuring that all drug and food products meet established safety and quality standards, thereby preventing harm to consumers.
The information that must be reported includes product details such as name, composition, dosage, intended use, manufacturing processes, and any safety evaluation findings related to the drug or food product.
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