01 1Chengdu Easton Biopharmaceuticals Co. , Ltd.
02 1DONGBANG FUTURE TECH & LIFE CO. , LTD.
03 1Fuji Chemical Industry Co., Ltd.
04 1Sanyo Chemical Research Institute Co., Ltd.
05 1Shiono Finesse Co., Ltd.
06 1UBE Inc.
07 1Zhejiang Tianyu Pharmaceutical Co. , Ltd.
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PharmaCompass offers a list of Silodosin 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 Silodosin manufacturer or Silodosin supplier for your needs.
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PharmaCompass also assists you with knowing the Silodosin API Price utilized in the formulation of products. Silodosin API Price is not always fixed or binding as the Silodosin Price is obtained through a variety of data sources. The Silodosin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KAD-3213, KMD-3213 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KAD-3213, KMD-3213, including repackagers and relabelers. The FDA regulates KAD-3213, KMD-3213 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KAD-3213, KMD-3213 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 KAD-3213, KMD-3213 supplier is an individual or a company that provides KAD-3213, KMD-3213 active pharmaceutical ingredient (API) or KAD-3213, KMD-3213 finished formulations upon request. The KAD-3213, KMD-3213 suppliers may include KAD-3213, KMD-3213 API manufacturers, exporters, distributors and traders.
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The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The KAD-3213, KMD-3213 Drug Master File in Japan (KAD-3213, KMD-3213 JDMF) empowers KAD-3213, KMD-3213 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the KAD-3213, KMD-3213 JDMF during the approval evaluation for pharmaceutical products. At the time of KAD-3213, KMD-3213 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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We have 6 companies offering KAD-3213, KMD-3213
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