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How is the amount of alimony determined in cases of de facto custody in Ecuador?
In cases of de facto custody, the amount of alimony is determined considering the needs of the child and the financial capacity of the non-custodial parent. Even if the relationship is not legally formalized, the court seeks to ensure that the child's needs are adequately met.
What are the penalties for revealing confidential information related to embargoes in El Salvador?
Disclosing confidential information related to seizures may result in sanctions including fines, civil liability for damages, and even legal action for violation of privacy or breach of professional duties.
What is the seizure process in cases of debts related to telephone services in Mexico?
The seizure process in cases of debts related to telephone services in Mexico involves notification of the debt, the request for seizure by the telephone company or the corresponding authority, the retention of accounts or assets, and the auction of assets if necessary to cover the debt. Specific procedures may vary depending on the jurisdiction and the nature of the debt.
What are the financial implications of the change in economic policies in Ecuador?
The change in economic policies may have significant financial implications in Ecuador. These policies can affect foreign investment, economic growth, inflation, interest rates, and monetary stability. It is essential to monitor and understand economic policies to adapt financial strategies and take advantage of emerging opportunities.
How is income obtained from the sale of intangible assets taxed in Argentina?
Income obtained from the sale of intangible assets is subject to Income Tax. Capital gain is determined by subtracting the original cost from the sale amount.
What are the laws in Panama that regulate clinical research and clinical trials, and what are the requirements and ethical standards that researchers and institutions that carry out these types of studies must meet?
Clinical research and clinical trials in Panama are regulated by laws such as Law 1 of 2001 on Medicines and Other Health Products. Ethical requirements and standards include obtaining informed consent from participants, approval from ethics committees, and notification to the health authority. The aim is to ensure the integrity and safety of the participants, as well as the validity and quality of the data generated in clinical research.
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