01 1Aragen Life Sciences Limited
01 1Pharmapia Co., Ltd.
01 1Sodium pentosan polysulfate
01 1India
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2022-06-15
Registration Number : 20220615-209-J-1314
Manufacturer Name : Aragen Life Sciences Limited
Manufacturer Address : Manufacturing Unit-I, Plot No. 28A, IDA, Nacharam Village, Uppal Mandal, Medchal - Ma...
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PharmaCompass offers a list of Pentosan Polysulfate Sodium 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 Pentosan Polysulfate Sodium manufacturer or Pentosan Polysulfate Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pentosan Polysulfate Sodium manufacturer or Pentosan Polysulfate Sodium supplier.
PharmaCompass also assists you with knowing the Pentosan Polysulfate Sodium API Price utilized in the formulation of products. Pentosan Polysulfate Sodium API Price is not always fixed or binding as the Pentosan Polysulfate Sodium Price is obtained through a variety of data sources. The Pentosan Polysulfate Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 37300-21-3 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 37300-21-3, including repackagers and relabelers. The FDA regulates 37300-21-3 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 37300-21-3 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of 37300-21-3 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 37300-21-3 supplier is an individual or a company that provides 37300-21-3 active pharmaceutical ingredient (API) or 37300-21-3 finished formulations upon request. The 37300-21-3 suppliers may include 37300-21-3 API manufacturers, exporters, distributors and traders.
click here to find a list of 37300-21-3 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a 37300-21-3 Drug Master File in Korea (37300-21-3 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 37300-21-3. The MFDS reviews the 37300-21-3 KDMF as part of the drug registration process and uses the information provided in the 37300-21-3 KDMF to evaluate the safety and efficacy of the drug.
After submitting a 37300-21-3 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 37300-21-3 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of 37300-21-3 suppliers with KDMF on PharmaCompass.
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