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What is the position of Colombian companies regarding hiring personnel with disciplinary backgrounds for inclusion and diversity roles?
In roles related to inclusion and diversity, some companies may adopt inclusive approaches, offering opportunities to people from disciplinary backgrounds who seek to contribute positively to the promotion of diversity in the workplace.
What is the role of legislative leaders and committees in the law-making process for regulatory compliance in El Salvador?
Leaders and committees have the responsibility of promoting bills, organizing debates and ensuring that the laws promoted strengthen regulatory compliance in the country.
What is the "right of lien" in a lease in Mexico?
The "right of lien" is the right of the landlord to retain personal property belonging to the tenant if the tenant fails to pay rent or fulfill his or her obligations. The lessor can retain the goods until the contract commitments are met.
How is the criminal responsibility of adolescents in conflict with the law regulated in Bolivia?
The criminal responsibility of adolescents in conflict with the law in Bolivia is regulated by specific juvenile justice regulations. It focuses on educational and social reintegration measures, avoiding severe sanctions and considering the stage of development of young people.
What is the legal framework in Costa Rica for the crime of minor injuries?
Minor injuries are punishable by law in Costa Rica. Those who cause minor physical harm to another person, which does not seriously endanger their life or physical integrity, may face legal action and sanctions, including fines and reparation measures to the victim.
What are the regulations related to the sale of pharmaceutical products in sales contracts in the Dominican Republic?
The sale of pharmaceutical products in the Dominican Republic is highly regulated by the General Directorate of Medicines, Food and Health Products (DIGEMAPS) and other authorities. Suppliers must comply with regulations related to the quality, safety, registration and labeling of pharmaceutical products to ensure the protection of public health. In contracts for the sale of pharmaceutical products, the parties must comply with these regulations and establish clauses to guarantee the legality and quality of the products. Contracts for the sale of pharmaceutical products must include detailed information about the products, their generic and trade names, indications for use, contraindications, side effects and any other information necessary to ensure the safe use of medicines. It is also essential to establish adverse event reporting procedures and responsibilities in case of quality or safety problems related to pharmaceutical products.
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