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2. Valid License to Operate of manufacturer/trader/distributor/importer
/exporter/wholesaler
3. Certificate of Brand Name Clearance
4. Agreement between
Importer/Exporter
Manufacturer
and
Trader
or
Distributor
5. General Information product's proprietary or brand name, official
chemical name(s) and generic name(s) of active ingredient(s),
molecular or chemical formula and structure, amount of active
ingredient per unit dose, pharmaceutical form of the drug,
indication, recommended dosage, frequency of administration, route
and mode of administration, contraindication, warnings and
precautions
6. Unit dose and batch formulation
Must be in full compliance with the latest official monograph
(United States Pharmacopeia, British Pharmacopeia, Japanese
Pharmacopeia,
European
Pharmacopeia,
International
Pharmacopeia); name and edition of the reference may be
cited in lieu of submitting a detailed list of limits and tests;
when an alternative procedure or limit is used, it shall be equal
to or more stringent than the official requirement
For non-official or unofficial substances, separate list of
technical specifications of each ingredient must include the ff:
Name of substance
detailed information on physical and chemical properties
ID tests
Purity tests
Assay
7. Technical/Quality Specifications
Packaging Materials
of
all
Raw
Materials
including
8. Certificate of Analysis of Active Ingredient(s)
9. Technical Specifications of the Finished Product
a) The appearance of the product (colour, shape dimensions,
4/21/2020, 9:19 AM
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