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Guidance on Application for License for Manufacturer Pharmaceutical Product (Secondary Packaging)Introduction Under the Pharmacy and Poisons Ordinance (Cap.138, Laws of Hong Kong), manufacture means
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Submit the filled-out application form and supporting documents to the relevant drug office as per the guidelines.
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Follow up with the drug office to track the progress of your application if necessary.
Who needs drug office - guidelines?
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Drug office guidelines are needed by individuals or organizations involved in the pharmaceutical industry.
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Anyone seeking to obtain licenses, permits, or approvals related to drugs or pharmaceutical products would require drug office guidelines to ensure compliance with regulations and guidelines set by the governing authorities.
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What is drug office - guidelines?
Drug office - guidelines refer to the regulations and instructions issued by the drug office regarding the proper handling and administration of pharmaceuticals.
Who is required to file drug office - guidelines?
Manufacturers, distributors, and retailers of pharmaceutical products are required to file drug office - guidelines.
How to fill out drug office - guidelines?
Drug office - guidelines can be filled out online on the drug office website or submitted in person at the drug office headquarters.
What is the purpose of drug office - guidelines?
The purpose of drug office - guidelines is to ensure the safe and effective use of pharmaceuticals, protect public health, and regulate the pharmaceutical industry.
What information must be reported on drug office - guidelines?
Drug office - guidelines must include information on product registration, labeling requirements, storage and distribution protocols, adverse event reporting procedures, and quality control measures.
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