01 1DSM Nutritional Products Ltd.
02 1F. Hoffmann-La Roche Limited.
01 2Cholecalciferol Cholecalciferol / Vitamin D3 Cr ystalline
01 1Netherlands
02 1Switzerland
Cholecalciferol / Vitamin D3 Crystalline
Registration Number : 218MF10105
Registrant's Address : Grenzacherstrasse 124, 4070 Basel, Switzerland
Initial Date of Registration : 2006-01-30
Latest Date of Registration : 2006-07-20
Cholecalciferol / Vitamin D3 Crystalline
Registration Number : 223MF10101
Registrant's Address : Wurmisweg 576, CH-4303, Kaiseraugst, Switzerland
Initial Date of Registration : 2011-07-11
Latest Date of Registration : 2011-07-11
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PharmaCompass offers a list of Vitamin D3 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 Vitamin D3 manufacturer or Vitamin D3 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin D3 manufacturer or Vitamin D3 supplier.
PharmaCompass also assists you with knowing the Vitamin D3 API Price utilized in the formulation of products. Vitamin D3 API Price is not always fixed or binding as the Vitamin D3 Price is obtained through a variety of data sources. The Vitamin D3 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CC manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CC, including repackagers and relabelers. The FDA regulates CC manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CC 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 CC manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CC supplier is an individual or a company that provides CC active pharmaceutical ingredient (API) or CC finished formulations upon request. The CC suppliers may include CC API manufacturers, exporters, distributors and traders.
click here to find a list of CC 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 CC Drug Master File in Japan (CC JDMF) empowers CC 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 CC JDMF during the approval evaluation for pharmaceutical products. At the time of CC 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 CC suppliers with JDMF on PharmaCompass.
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