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GUIDANCE DOCUMENT Labelling of Pharmaceutical Drugs for Human Unpublished by authority of the Minister of Healthcare Adopted2013/11/01Date Revised2015/06/13Effective Date2015/06/13Health Products
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LabelGuideld-engpdf refers to a regulatory document that outlines requirements for labeling and providing health protection information for drugs to ensure consumer safety and compliance with health regulations.
Pharmaceutical companies and manufacturers of drugs are required to file the labelguideld-engpdf to comply with health protection regulations.
To fill out the labelguideld-engpdf, companies must include specific information such as drug ingredients, usage instructions, safety warnings, and manufacturer details as per the regulatory guidelines.
The purpose of the labelguideld-engpdf is to ensure that consumers have access to essential health information regarding drugs, thereby promoting safety and informed use.
The information that must be reported includes drug composition, dosage recommendations, adverse effects, contraindications, and manufacturer's contact information.
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