01 1FORMOSA LABORATORIES, INC.
02 1MicroBiopharm Japan Co., Ltd.
03 1Shiono Finesse Co., Ltd.
01 2Calcitriol
02 1File Leka Rushito triol bulk powder
01 2Japan
02 1Taiwan
Registration Number : 228MF10187
Registrant's Address : 36 Hoping Street, Louchu, Taoyuan 33842, Taiwan
Initial Date of Registration : 2016-09-26
Latest Date of Registration : 2016-09-26
Registration Number : 223MF10117
Registrant's Address : 1-3-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2011-07-25
Latest Date of Registration : 2014-03-11
Registration Number : 218MF10427
Registrant's Address : 3-1-6 Doshomachi, Chuo-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2009-12-09
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PharmaCompass offers a list of Calcitriol 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 Calcitriol manufacturer or Calcitriol supplier for your needs.
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PharmaCompass also assists you with knowing the Calcitriol API Price utilized in the formulation of products. Calcitriol API Price is not always fixed or binding as the Calcitriol Price is obtained through a variety of data sources. The Calcitriol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol, including repackagers and relabelers. The FDA regulates (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol 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 (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol supplier is an individual or a company that provides (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol active pharmaceutical ingredient (API) or (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol finished formulations upon request. The (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol suppliers may include (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol API manufacturers, exporters, distributors and traders.
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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 (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol Drug Master File in Japan ((5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol JDMF) empowers (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol 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 (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol JDMF during the approval evaluation for pharmaceutical products. At the time of (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol 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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We have 3 companies offering (5Z,10-secocholesta-5,7,10(19)-triene-1.alpha.,3.beta.,25-triol
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