01 2BASF SE
01 1CTC Bio Co., Ltd.
02 1Parmarine Co., Ltd.
01 2Calcium pantothenate
01 2Germany
Registrant Name : CTC Bio Co., Ltd.
Registration Date : 2022-05-02
Registration Number : 20220502-211-J-1281
Manufacturer Name : BASF SE
Manufacturer Address : Carl-Bosch-Strasse 38, 67056 Ludwigshafen, Germany
Registrant Name : Parmarine Co., Ltd.
Registration Date : 2025-05-12
Registration Number : 20220502-211-J-1281(1)
Manufacturer Name : BASF SE
Manufacturer Address : Carl-Bosch-Strasse 38, 67056 Ludwigshafen, Germany
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PharmaCompass offers a list of Calcium Pantothenate 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 Calcium Pantothenate manufacturer or Calcium Pantothenate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcium Pantothenate manufacturer or Calcium Pantothenate supplier.
PharmaCompass also assists you with knowing the Calcium Pantothenate API Price utilized in the formulation of products. Calcium Pantothenate API Price is not always fixed or binding as the Calcium Pantothenate Price is obtained through a variety of data sources. The Calcium Pantothenate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A P2250_SIAL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of P2250_SIAL, including repackagers and relabelers. The FDA regulates P2250_SIAL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. P2250_SIAL 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 P2250_SIAL supplier is an individual or a company that provides P2250_SIAL active pharmaceutical ingredient (API) or P2250_SIAL finished formulations upon request. The P2250_SIAL suppliers may include P2250_SIAL API manufacturers, exporters, distributors and traders.
click here to find a list of P2250_SIAL 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 P2250_SIAL Drug Master File in Korea (P2250_SIAL KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of P2250_SIAL. The MFDS reviews the P2250_SIAL KDMF as part of the drug registration process and uses the information provided in the P2250_SIAL KDMF to evaluate the safety and efficacy of the drug.
After submitting a P2250_SIAL 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 P2250_SIAL API can apply through the Korea Drug Master File (KDMF).
click here to find a list of P2250_SIAL suppliers with KDMF on PharmaCompass.
