SWATI - Transforming science into solutions with 60+ years of expertise, global accreditations, and pioneering biotech innovation.
01 1Swati Spentose Private Limited (Unit-I)
02 2Dongbang FTL Co., Ltd.
03 1Engchem Life Sciences Co., Ltd.
04 1Fuji Chemical Industries Co., Ltd.
05 1Hanseochem Co., Ltd.
06 1Inistest Co., Ltd.
07 1Metrochem API Pvt Ltd, Unit- IV
08 1Shiono Finesse, Ltd. Fukui Factory
09 1URQUIMA SA
10 1Zhejiang Tianyu Pharmaceutical Co., Ltd.
SWATI - Transforming science into solutions with 60+ years of expertise, global accreditations, and pioneering biotech innovation.
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2024-06-28
Registration Number : Su258-20-ND
Manufacturer Name : Swati Spentose Private Limit...
Manufacturer Address : Plot No. A-1/2102 & 2103, Phase III, GIDC, VAPI - 396 195 Dist.- Valsad, Gujarat Stat...
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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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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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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a KAD-3213, KMD-3213 Drug Master File in Korea (KAD-3213, KMD-3213 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of KAD-3213, KMD-3213. The MFDS reviews the KAD-3213, KMD-3213 KDMF as part of the drug registration process and uses the information provided in the KAD-3213, KMD-3213 KDMF to evaluate the safety and efficacy of the drug.
After submitting a KAD-3213, KMD-3213 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 KAD-3213, KMD-3213 API can apply through the Korea Drug Master File (KDMF).
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We have 8 companies offering KAD-3213, KMD-3213
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