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Профиль для :: caythuoc
Аватар Обо мне caythuoc
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Дата регистрации:  08/04/2021 05:38:51
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Вебсайт:  http://lispharma.vn/
Интересы: https://bikipsongkhoe.wordpress.com/2020/10/11/cac-duoc-lieu-thien-nhien-thuong-dung-cho-van-de-tieu-hoa/ https://bikipsongkhoe.wordpress.com/2020/10/
Биография: Lis Cosmetics Pharmaceutical Joint Stock Company is a unit operating in the field of providing: functional food processing , Production and processing of cosmetics, Production and processing of traditional drugs, supply biotechnological materials and active ingredients from nature; finished products, functional foods, pharmaceuticals, food and cosmetics... Address: Adjacent to 16-19, New Urban Area, An Hung, La Khe Ward, Ha Dong District, Hanoi City Website: https://lispharma.vn/pages/gia-cong-sua-bot MST/DKKD/QDTL: 0105716834 Mail: nhamaysxtpcn@gmail.com Hotline: 0329016668 / 0989386863 #Lis #giacongthucphamchucnang More about the best GMP Lisgroup standard functional food processing factory today: Currently, one of the best standards in consulting "outsourcing functional foods" is the GMP (Good Manufacturing Practice) Standard of the European Federation for Pharmaceutical Industries and Associations (EFPIA). . This is a system of high quality management standards applied in the functional food manufacturing process to ensure the safety, effectiveness and quality of the product. EFPIA's GMP standards include requirements for infrastructure, equipment, manufacturing processes, quality control, materials management, document management, process management, and staff training. pellets. It also requires compliance with laws and regulations related to the production of dietary supplements. In addition, there are a number of other national GMP standards that are globally applied, including: GMP standard of the US Food and Drug Administration (FDA). GMP standard of the Canadian Pharmaceutical and Medical Devices Association (Health Canada). GMP standard of the World Health Organization (WHO). GMP standard of the European Medicines Agency (EMA). These standards all have the common goal of ensuring safe, effective and quality functional food processing. However, determining the best standard depends on many factors, including the size, industry, and the specific legal and regulatory requirements of the country where the outsourcing plant is located. Therefore, when choosing GMP standards, your company should learn and comply with the requirements suitable to your location and business requirements. Processing process of tpcn tablets according to GMP standards of functional food factories: The process of processing functional foods in tablet form according to GMP (Good Manufacturing Practice) standards is usually done according to the following steps: Formulation design: The first step is to design a formula for a functional food tablet. This includes the selection of raw materials, determination of the content and composition of each ingredient, as well as the determination of production technology and related specifications. Prepare ingredients: The ingredients are prepared according to the designed recipe. Ensure that raw materials are tested and meet quality requirements before use. Equipment preparation: Tablet production equipment, including tablet presses, pellet machines, conveying systems, and other equipment should be prepared and inspected prior to use. Make sure they work correctly and meet the requirements of the GMP standard. Work Surface Preparation: Work surfaces, including desks, equipment and work areas, should be cleaned and prepared to ensure hygiene and safety during production. Production of tablets: The production process of functional food tablets includes the following steps: Dissolve and mix ingredients: The ingredients are dissolved and mixed to create a material mixture. Tablets: The mixture of materials is compressed by a pellet machine to create tablets. Quality control: Tablets are sampled for quality testing, including testing for weight, hardness, strength, active ingredient dispersion, and other GMP requirements. Packaging: The high quality tablets are packaged in appropriate packaging, ensuring their preservation and safety. Storage and transport: After the tablets are manufactured, they need to be stored and transported properly to ensure that their quality is not affected. This includes storing the tablets under suitable conditions, protection from sunlight, and suitable temperature and humidity. When transporting, it is necessary to comply with regulations on preservation and transportation of functional food products. Recording and reporting: In the tablet supplement manufacturing process, important information related to tablet production, including material specifications, quality control data and control measures, is required. control, should be fully recorded and reported. This helps to monitor the production process, identify problems and take corrective action if necessary. Periodic maintenance and inspection: Tablet production systems and equipment need to be maintained and checked periodically to ensure stable and accurate operation. Maintenance procedures are designed to inspect, clean, repair and upgrade equipment as needed. Employee training: Ensure that employees involved in the processing of dietary supplements in tablet form fully meet the requirements of GMP standards. Employee training in production processes, hygiene regulations, quality management and safety requirements is important to ensure product quality and GMP compliance. Factory1: https://naturepharma.net.vn/ Factory2: http://tadaphaco.vn/
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