01 1DSM Nutritional Products Ltd.
01 1Calcium pantothenate Calcium D-Pantothenate
01 1Netherlands
Registration Number : 217MF11286
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2005-12-22
Latest Date of Registration : 2006-11-21
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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.
click here to find a list of P2250_SIAL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
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.
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 P2250_SIAL Drug Master File in Japan (P2250_SIAL JDMF) empowers P2250_SIAL 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 P2250_SIAL JDMF during the approval evaluation for pharmaceutical products. At the time of P2250_SIAL 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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