01 1Union Quimica Farmaceutica SA
01 1Ipsen Korea Co., Ltd.
01 1Hexaminolevulinate hydrochloride
01 1Spain
Hexaminolevulinate hydrochloride
Registrant Name : Ipsen Korea Co., Ltd.
Registration Date : 2008-05-07
Registration Number : 3231-1-ND
Manufacturer Name : Union Quimica Farmaceutica S...
Manufacturer Address : Poligon Industrial Moli de les Planes, Font de Bocs S/N 08470, Sant Celoni, Barcelona
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PharmaCompass offers a list of Aminolevulinic Acid Hexylester API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Aminolevulinic Acid Hexylester manufacturer or Aminolevulinic Acid Hexylester supplier for your needs.
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PharmaCompass also assists you with knowing the Aminolevulinic Acid Hexylester API Price utilized in the formulation of products. Aminolevulinic Acid Hexylester API Price is not always fixed or binding as the Aminolevulinic Acid Hexylester Price is obtained through a variety of data sources. The Aminolevulinic Acid Hexylester Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A hexaminolevulinate HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of hexaminolevulinate HCl, including repackagers and relabelers. The FDA regulates hexaminolevulinate HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. hexaminolevulinate HCl API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A hexaminolevulinate HCl supplier is an individual or a company that provides hexaminolevulinate HCl active pharmaceutical ingredient (API) or hexaminolevulinate HCl finished formulations upon request. The hexaminolevulinate HCl suppliers may include hexaminolevulinate HCl API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a hexaminolevulinate HCl Drug Master File in Korea (hexaminolevulinate HCl KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of hexaminolevulinate HCl. The MFDS reviews the hexaminolevulinate HCl KDMF as part of the drug registration process and uses the information provided in the hexaminolevulinate HCl KDMF to evaluate the safety and efficacy of the drug.
After submitting a hexaminolevulinate HCl KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their hexaminolevulinate HCl API can apply through the Korea Drug Master File (KDMF).
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