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   1 
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   Notifying Member 
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   Macao, China 
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   2 
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   Title of new
  legislation/procedure 
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   Import Licence
  Application for Glands and Other Organs for Organo-therapeutic Uses, Blood
  Plasma, Human Blood, and Animal Blood  
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   3 
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   Date of Publication 
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   15 August 2024 
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   4 
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   Date of entry into force 
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   15 August 2024 
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   5 
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   Website link/Official
  publication of the new regulation/procedure 
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   https://www.gov.mo/en/services/ps-2190/ 
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   6 
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   Have you attached a copy of the
  regulation (PDF) to the Secretariat 
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   [X] Yes. (Please attach a copy of the regulation to the notification.) 
    
  [ ] No. 
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   7 
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   Type of notification 
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   [X] (a) New
  licensing regulation/procedure[2];
  (please answer question 8 to 14) 
    
  [ ] (b) Changes
  to a regulation/procedure which has been previously notified in document: _________
  (please answer question 15 and 16) 
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   8 
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   List of products subject to
  licensing 
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   ex. 3001.90.90, ex.
  3002.12.10, ex. 3002.12.90, ex. 3002.90.30, ex. 3002.90.40 
  "ex." means
  "part of" 
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   9 
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   Nature of licensing 
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   Automatic: [ ] 
    
  Non-Automatic: [X] 
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   10 
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   Administrative purpose/measure
  being implemented 
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   (a) 
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   Protect public morals; 
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   (b) 
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   Protect human, animal or plant life and health;
  protect environment; 
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   (c) 
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   Collect trade statistics or market surveillance; 
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   (d) 
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   Protection of patents, trademarks and copyrights, and
  the prevention of deceptive practices; 
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   (e) 
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   Pursue obligations under the UN Charter and other
  international treaties (i.e. CITES, Basel
  Convention, Rotterdam Convention, UNSC Resolutions etc.) 
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   (f) 
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   Quota (including TRQ) administration; 
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   (g) 
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   Regulate imports of arms, ammunition or fissionable
  materials and safeguard national security; 
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   (h) 
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   Other: ______________ (please
  specify) 
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   11 
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   Administrative body(ies) for 
  submission of applications  
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   Centre for Disease
  Prevention and Control, Health Bureau, Macao SAR 
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   12 
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   Contact point for information
  on eligibility 
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   Ministry/authority and
  Department: Centre for Disease Prevention and Control, Health Bureau, Macao
  SAR 
  Address:
  Avenida do Comendador Ho Yin, Edf. de Escritóriios do Governo(Qingmao), 18
  andar, Macao 
  Website: https://www.ssm.gov.mo/Portal/portal.aspx?lang=pt 
  Telephone: (853) 2853
  3525 
  E-Mail: cdc@ssm.gov.mo 
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   13 
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   Expected duration of licensing
  procedure 
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   The prior
  authorization application can be issued within 15 working days, and the
  import licence will be issued within 2 working days. 
   | 
 
 
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   14 
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   A
  summary of the notification in one of the WTO official languages  
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   According to Article 3-A of Administrative Regulation
  No. 28/2003 – Regulations on External Trade Activities and Article 9 of the
  External Trade Law (Law No. 7/2003), the Health Bureau, Macao SAR is vested
  with the authority to issue import licences for the following goods: Glands
  and other organs for organo-therapeutic uses, blood plasma, human blood,
  animal blood, which are indicated in Group B2 of Table B. 
   | 
 
 
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   15 
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   In
  the case of 7(b), please indicate the type of new change(s) 
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     (a) 
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     Termination 
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     (b) 
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     Suspension 
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     (c) 
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     Modification of specific
    details in existing  
    procedures: 
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    | 
      
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     Product coverage; 
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     Administrative
    purpose; 
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     Automatic or
    Non-automatic; 
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     Duration of
    licensing; 
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     Change the nature of
    quantity/value restriction; 
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    | 
      
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     Eligibility of
    applicants; 
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     Contact information
    on eligibility; 
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     Administrative
    body(ies) for submission of application; 
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     Documentation
    requirements (including application form); 
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     Period for
    Application; 
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     Administrative
    body(ies) to issue licence; 
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     Processing time for
    issuing licence; 
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     Licence
    fee/administrative charge; 
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     Deposit/advance
    payment and relevant conditions; 
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     Appeal
    regulations/procedures; 
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     Validity of licence; 
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     Other conditions of
    licence (extension, transferability, penalty of non-use etc.); 
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     Foreign exchange
    requirements; 
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     Other: __________
    (please specify). 
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     | 
     | 
     | 
    
   
   
   
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   16  
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   Please
  elaborate the changes in detail (in one of the WTO official languages) 
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