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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A DSSTox_RID_78090 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_RID_78090, including repackagers and relabelers. The FDA regulates DSSTox_RID_78090 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_RID_78090 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 DSSTox_RID_78090 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A DSSTox_RID_78090 supplier is an individual or a company that provides DSSTox_RID_78090 active pharmaceutical ingredient (API) or DSSTox_RID_78090 finished formulations upon request. The DSSTox_RID_78090 suppliers may include DSSTox_RID_78090 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_RID_78090 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 DSSTox_RID_78090 Drug Master File in Japan (DSSTox_RID_78090 JDMF) empowers DSSTox_RID_78090 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 DSSTox_RID_78090 JDMF during the approval evaluation for pharmaceutical products. At the time of DSSTox_RID_78090 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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