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REPUBLIC OF SOUTH AFRICAIN THE HIGH COURT OF SOUTH AFRICA GAUTENG DIVISION, PRETORIA Case Number: A87/2023 (1) (2) (3)REPORTABLE: NO OF INTEREST TO OTHER JUDGES: NO REVISED: NOIn___ the matter between:___
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How to fill out central drug authority

01
Gather all necessary information and documentation related to the drug
02
Complete the required application form accurately
03
Submit the application form along with supporting documents to the central drug authority
04
Wait for the central drug authority to review and process the application
05
Comply with any additional requirements or requests for information from the authority

Who needs central drug authority?

01
Pharmaceutical companies seeking approval for new drugs
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Manufacturers of medical devices requiring regulatory approval
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Researchers conducting clinical trials involving drugs
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The central drug authority is a regulatory body responsible for overseeing the approval, manufacture, distribution, and control of drugs in a particular country.
Pharmaceutical companies, drug manufacturers, and distributors are required to file central drug authority.
To fill out central drug authority, one must provide detailed information about the drug being manufactured or distributed, including its composition, intended use, and potential side effects.
The purpose of central drug authority is to ensure the safety, efficacy, and quality of drugs available in the market for public use.
Information such as the name of the drug, its active ingredients, dosage form, and packaging must be reported on central drug authority.
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