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What is the validity period of an emergency passport in Panama?
The emergency passport in Panama has a limited validity, generally a few months or until the emergency trip is completed. After returning, you must apply for a regular passport.
What is the role of the government in regulating lease contracts in Panama?
The government of Panama has a regulatory role to establish laws and regulations that govern lease contracts, ensuring the protection of the rights of both the landlord and the tenant.
What is the situation of the implementation of renewable energy in rural areas of Honduras?
The implementation of renewable energy in rural areas of Honduras has advanced in recent years, with rural electrification projects based on sources such as solar, wind and hydroelectric energy. These initiatives have contributed to improving access to electricity in remote communities and reducing dependence on fossil fuels. However, challenges remain in terms of equitable access, sustainability and maintenance of renewable energy infrastructure in rural areas.
What is the impact of migration on labor productivity in Mexico?
Migration can impact labor productivity in Mexico by affecting labor supply, professional specialization, and competition in the labor market in areas of origin and destination of migrants, which can influence the country's efficiency, innovation, and economic development. .
What is the impact of drug policies on indigenous communities in Costa Rica?
Drug policies can have specific impacts on indigenous communities in Costa Rica, and culturally sensitive approaches are being implemented to address these issues and promote inclusive solutions.
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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