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| Regulatory Issues |
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Good Manufacture Practices
Neo Química is qualified by the Certificate of Good Manufacture Practices (BPF), which guarantees that the company fulfills with all the norms demanded by the legislation of the pharmaceutical sector to medicine manufacture. The Good Manufacture Practices norms constitute an important tool of the quality guarantee system. They define and standardize methods that regulate the activities of products manufacture, which involves the participation of the people, production process, conditions of equipment, raw materials, packaging, maintenance, environment security and protection, storage, the expedition until its distribution and transport.
According to the RDC # 210, August 4, 2003, "registered medicines must be produced only by licensed manufacturers, holders of Authorization to Manufacture, who have their activities regularly inspected by the competent National Sanitary Authorities". Neo Química follows the norms established by the Good Manufacture Practices, thus aiming to answer all the legislation that regulates the sector. It is the social commitment with the quality and excellence in high quality products manufacture that follows requirements such as security and concentration, overall, the manufacture technical requirements.
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