01 1Ajinomoto Co., Inc.
02 2Prime European Therapeuticals S. p. A. (Euticals S.p.A.)
03 1Yamasa Soy Sauce Co., Ltd.
01 1"Outsider Regulations" vidarabine (production only)
02 1Outsiders regulations vidarabine (production only)
03 1Vidarabine
04 1Vidarabine "Ajinomoto"
01 2Italy
02 2Japan
Registration Number : 217MF10300
Registrant's Address : 1-15-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-06-30
Latest Date of Registration : 2010-03-23
Registration Number : 227MF10026
Registrant's Address : Viale Bianca Maria 25-20122 Milano-Italy
Initial Date of Registration : 2015-01-23
Latest Date of Registration : 2015-01-23
"Extra-official" vidarabine (for manufacturing purposes only)
Registration Number : 218MF10132
Registrant's Address : Viale Bianca Maria 25-20122 Milano-Italy
Initial Date of Registration : 2006-01-30
Latest Date of Registration : 2008-02-25
Extramural regulations Vidarabine (for manufacturing only)
Registration Number : 218MF10480
Registrant's Address : 2-10-1 Shinseicho, Choshi City, Chiba Prefecture
Initial Date of Registration : 2006-05-15
Latest Date of Registration : 2009-01-28
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PharmaCompass offers a list of Vidarabine 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 Vidarabine manufacturer or Vidarabine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vidarabine manufacturer or Vidarabine supplier.
PharmaCompass also assists you with knowing the Vidarabine API Price utilized in the formulation of products. Vidarabine API Price is not always fixed or binding as the Vidarabine Price is obtained through a variety of data sources. The Vidarabine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A alpha Ara A manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of alpha Ara A, including repackagers and relabelers. The FDA regulates alpha Ara A manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. alpha Ara A 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 alpha Ara A supplier is an individual or a company that provides alpha Ara A active pharmaceutical ingredient (API) or alpha Ara A finished formulations upon request. The alpha Ara A suppliers may include alpha Ara A 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 alpha Ara A Drug Master File in Japan (alpha Ara A JDMF) empowers alpha Ara A 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 alpha Ara A JDMF during the approval evaluation for pharmaceutical products. At the time of alpha Ara A 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 alpha Ara A suppliers with JDMF on PharmaCompass.
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