Legislation on Counterfeit Medicines in the region

Lorem Ipsum Dolor

Information

Type

Cuestionario

Version

File Size

4.00 KB

Published Date

01/01/2017

Period

Previous

Categoría

ASIPI Writes,Previous Periods

Authors

ASIPI

Attached Files:

MASTER_FINAL.pdf

Addendum-Anexo-No-1-Argentina.pdf

Addendum-Anexo-No-2-Belize.pdf

Addendum-Anexo-No-3-Bolivia.pdf

Addendum-Anexo-No-4-Costa-Rica.pdf

Addendum-Anexo-No-5-Brazil.pdf

Addendum-Anexo-No-6-Chile.pdf

Addendum-Anexo-No-7-Colombia.pdf

Addendum-Anexo-No-8-Ecuador.pdf

Addendum-Anexo-No-09-El-Salvador.pdf

Addendum-Anexo-No-10-Guatemala.pdf

Addendum-Anexo-No-11-Honduras.pdf

Addendum-Anexo-No-12-Mexico.pdf

Addendum-Anexo-No-13-Nicaragua.pdf

Addendum-Anexo-No-14-Panama.pdf

Addendum-Anexo-No-15-Paraguay.pdf

Addendum-Anexo-No-16-Peru.pdf

Addendum-Anexo-No-17-Republica-Dominicana.pdf

Addendum-Anexo-No-18-Uruguay.pdf

Addendum-Anexo-No-19-Venezuela.pdf


REGULATION AGAINST THE COUNTERFEITING OF PHARMACEUTICAL PRODUCTS IN LATIN AMERICA

  1. REGULATORY FRAMEWORK
  2. AUTHORITIES
  3. PASSABLE SUBJECTS OF PENALTY
  4. TYPE OF SANCTIONS
  5. FALSIFIED GOODS DESTINATION SEIZED AT THE END OF THE PROCESS
  6. PRECAUTIONARY MEASURES (MC)
  7. MEASURES IN BORDER

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