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
A Calcium Pantothenate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Calcium Pantothenate, including repackagers and relabelers. The FDA regulates Calcium Pantothenate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Calcium Pantothenate 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 Calcium Pantothenate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Calcium Pantothenate supplier is an individual or a company that provides Calcium Pantothenate active pharmaceutical ingredient (API) or Calcium Pantothenate finished formulations upon request. The Calcium Pantothenate suppliers may include Calcium Pantothenate API manufacturers, exporters, distributors and traders.
click here to find a list of Calcium Pantothenate 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 Calcium Pantothenate Drug Master File in Japan (Calcium Pantothenate JDMF) empowers Calcium Pantothenate 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 Calcium Pantothenate JDMF during the approval evaluation for pharmaceutical products. At the time of Calcium Pantothenate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Calcium Pantothenate suppliers with JDMF on PharmaCompass.
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