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What is the legislation in Guatemala regarding assisted reproduction and in vitro fertilization?
Legislation on assisted reproduction and in vitro fertilization in Guatemala is limited. There are no specific laws that regulate these procedures, which can generate legal uncertainty. It is recommended to seek legal advice.
Are there restrictions on the sale of cultural or historical goods in Panama?
Yes, the sale of cultural or historical property may be subject to specific regulations and restrictions to protect the country's cultural heritage.
What is the procedure to obtain a newborn's ID?
To obtain the DNI of a newborn, the birth certificate must be presented at the Civil Registry and then complete the process at Renaper. It is advisable to start this process in the first months of life.
What is the National Infrastructure Program for Competitiveness in Peru?
The National Infrastructure Program for Competitiveness aims to promote the development of infrastructure in Peru to improve the country's competitiveness. Through construction projects, improvement and maintenance of transportation, energy, telecommunications and other sectors infrastructure, we seek to strengthen connectivity, reduce logistics costs and promote economic growth.
Is there a clear definition of “politically exposed person” (PEP) in Guatemalan AML legislation?
Yes, Guatemala's AML legislation provides a clear definition of "politically exposed person" (PEP), including government officials and persons with relevant public positions, as well as their close family members and associates.
What is the role of the Panamanian Agency for Medicines and Health Technologies (AUPSA) in the regulation of judicial files related to pharmaceutical products and medical technologies in Panama?
The Panamanian Agency for Medicines and Health Technologies (AUPSA) has an important role in the regulation of judicial files related to pharmaceutical products and medical technologies in Panama. Contributes to establishing regulations and policies for the management of files linked to the approval, control and marketing of products in the health sector. Their participation ensures transparency and legality in judicial matters related to the health industry, protecting the rights of citizens and contributing to the safety and effectiveness of medical products in the country.
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