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How are returns of non-conforming products handled in Bolivia?
The handling of returns of non-conforming products is regulated in clause [Clause Number], specifying the steps and procedures that the buyer and seller must follow to address and resolve returns related to products that do not meet specifications in Bolivia.
What is the deadline to file a complaint for improper embargo in Argentina?
The deadline to file a claim for improper seizure in Argentina is generally five years from the time the seizure occurred. It is important to file the complaint with the appropriate court and present the necessary evidence to support the claim of wrongful seizure.
How are international sales contracts approached in Guatemala and what international regulations apply?
International sales contracts in Guatemala may be governed by the United Nations Convention on Contracts for the International Sale of Goods (CISG), which Guatemala has ratified. These international regulations provide uniform rules for international sales, including aspects such as the formation of the contract, obligations of the parties and remedies in case of non-compliance.
What is the protection of the rights of people in situations of forced disappearance of people in Colombia?
People in situations of forced disappearance in Colombia have protected rights. These rights include the right to the truth, the right to justice, the right to comprehensive reparation, the right to identity and the right to search and locate missing persons.
Can I apply for temporary residence in Spain as a volunteer in social projects as an Ecuadorian?
Yes, temporary residence permits can be requested for volunteers in social projects. You must have an offer to participate in a recognized project and meet the established requirements.
How is due diligence addressed in mergers and acquisitions of companies in the pharmaceutical sector in Peru, considering health and intellectual property regulations?
Due diligence in companies in the pharmaceutical sector in Peru involves the review of health regulations, certifications of good manufacturing practices and intellectual property rights. Compliance records, patents, and potential intellectual property litigation are analyzed. In addition, the company's ability to adapt to changes in health legislation and innovation in pharmaceutical products is evaluated.
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