1. name of pharmacopoeia - who.int · the role of the formulário galénico português (portuguese...
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1. Name of pharmacopoeia
FARMACOPEIA PORTUGUESA PORTUGUESE PHARMACOPOEIA
(including the translation of the European Pharmacopoeia)
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2. Pharmacopoeia referred to in national/regional legislations
Besides being obviously referred in the legislation from Portugal, it is also accepted in the legislation from Brasil and other countries where Portuguese is an official language (Moçambique, Guiné or S.Tomé e Princípe, for instance)
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National/regional legislation includes reference to other
National Pharmacopoeias
United States Pharmacopoeia, Pharmacopoeia of Japan, British Pharmacopoeia or any other pharmacopoeia from an European country
Regional Pharmacopoeias - No
International Pharmacopoeias
European Pharmacopoeia
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4. Publication of latest edition
The Farmacopeia Portuguesa 9 was published from 2008 until 2011
The publication of Farmacopeia Portuguesa 10 will start during 2012
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5. Update frequency
As the European Pharmacopoeia, Farmacopeia Portuguesa is published every four years, with three supplements each year
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6. For which products does the pharmacopoeia provide specifications?
APIs Dosage forms – Human and Veterinary use Herbal products Biologicals
The role of the Formulário Galénico Português (Portuguese Galenic Formulary)
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7. Number of texts included in the pharmacopoeia
monographs for APIs – Ph.Eur.
monographs for finished dosage forms: about 85
monographs for biologicals – Ph.Eur.
general monographs – Ph.Eur.
supplementary texts – Ph.Eur. and a text concerning the use of coloring agents in dosage forms
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8. Collaboration with and/or being part of a (different) national/regional pharmacopoeia
No
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9. Publication of harmonized pharmacopoeial texts within the pharmacopoeia
. Only the harmonized texts included in the European Pharmacopoeia
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10. Interaction with stakeholders, including regulators
Interaction with the portuguese regulators
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11. Strategy for the future
– To continue the colaboration with the European Pharmacopoeia
– To update the national texts
– To tighten the links with the Portuguese speaking countries
– To tighten the links with stakeholders (regulators, manufacturers of APIs and manufacturers of medicines).