Pharmaceutical products: Zuclopenthixol decanoate, solution for injection, 200 mg/ml, ampoule 1 ml

The product must be properly registered in Ukraine in the manner prescribed by law and meet national and/or international standards. Medicines are delivered at the Supplier's expense in accordance with the Customer's application. The supplier must have all the necessary permits for the right to sell to health care institutions and supply the product with documentary evidence of the medicinal product's compliance, namely: copies of registration certificates or copies of state registration certificates; copies of quality certificates of each series of the medicinal product regarding dosage, dosage form, series number, quantity, name of the manufacturer of the medicinal product, as well as invoices. The release form, dosage and other parameters must correspond to those specified in the purchase. The supplier must ensure proper conditions for storage and transportation of medicinal products in compliance with the conditions of the "cold chain". Containers and packaging must meet the requirements established for this type of product and protect the medicinal product from damage and deterioration during transportation. The shelf life of medicinal products at the time of product delivery must be at least 80% of the total shelf life determined by the manufacturer. At the time of delivery of the goods, together with the primary documents, the Supplier provides a document confirming the expiration date of the goods. The price of the goods, which is the subject of the purchase, must take into account all taxes and fees paid or to be paid in relation to the offered goods, taking into account insurance, loading and unloading works, payment of customs tariffs and all other costs related to the execution of the Agreement