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Import of Goods (Pharmaceutical Administration Bureau)

Prior Authorisation for Import of Special Milk for Infants


How to Apply

Time of application: Before applying for the import licence for special milk for infants (i.e. infant formula milk powder), the applicant must first obtain the relevant prior authorisation for import from the Pharmaceutical Administration Bureau.

Eligibility: Businesses holding the “Registration for Controlled Foreign Trade Operations” issued by the Economic and Technological Development Bureau.

Application procedures and documents required:

In submitting application to import special milk for infants (i.e. infant formula milk powder), the following document and information are required:

  • Certificate of free sale or health certificate of the relevant product issued by the country of origin or a competent authority, the health certificate must contain the batch number and expiration date of the product under application;
  • Outer package;
  • “Infant formula nutrition table”[pdf] issued by the manufacturer;
  • A relevant “prior authorisation”[pdf][doc] must be completed for each import application.

Location of Application and Service Hours

Location of application: Pharmaceutical Administration Bureau

Address: Avenida do Comendador Ho Yin, Edifício de Escritórios do Governo (Qingmao), 19.º andar, Macau

Service hours:

Mondays to Thursdays: 09:00-13:00; 14:30-17:45

Fridays: 09:00-13:00; 14:30-17:30

Closed on Saturdays, Sundays and public holidays


Fees

Free of charge


Application Processing Time

The prior authorisation will be issued in 3 working days upon receipt of all required documents. (Performance Pledge)

The import license will be issued on the same day. (Performance Pledge)


Relevant Specifications or Requirements

Law no. 7/2003 – Foreign Trade Law

Chief Executive Dispatch no. 209/2021 – List of Goods Authorised for Importation

Administrative Regulation no. 28/2016 – Nutrient Requirements for Infant Formulas


Application Status Enquiry and Result Collection

Method of result collection: In person


Content provider: Pharmaceutical Administration Bureau (ISAF)

Last modified: 2024-07-11 10:56

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