Xellia Delivering Reliable Anti-Infective Solutions Through Expertise, Quality, and Uninterrupted Global Supply.
01 1Xellia (Taizhou) Pharmaceuticals Co. ,Ltd
01 1Japanese Pharmacopoeia bacitracin
01 1Denmark
Xellia Delivering Reliable Anti-Infective Solutions Through Expertise, Quality, and Uninterrupted Global Supply.
Japanese Pharmacopoeia Bacitracin
Registration Number : 225MF10193
Registrant's Address : １０８ Ｂｉｎｈａｉ Ｒｏａｄ， Ｔａｉｚｈｏｕ， Ｚｈ...
Initial Date of Registration : 2013-10-09
Latest Date of Registration : 2013-10-09
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PharmaCompass offers a list of Bacitracin Zinc API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Bacitracin Zinc manufacturer or Bacitracin Zinc supplier for your needs.
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A ZIBA-RX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ZIBA-RX, including repackagers and relabelers. The FDA regulates ZIBA-RX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ZIBA-RX 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 ZIBA-RX manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A ZIBA-RX supplier is an individual or a company that provides ZIBA-RX active pharmaceutical ingredient (API) or ZIBA-RX finished formulations upon request. The ZIBA-RX suppliers may include ZIBA-RX API manufacturers, exporters, distributors and traders.
click here to find a list of ZIBA-RX 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 ZIBA-RX Drug Master File in Japan (ZIBA-RX JDMF) empowers ZIBA-RX 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 ZIBA-RX JDMF during the approval evaluation for pharmaceutical products. At the time of ZIBA-RX 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 ZIBA-RX suppliers with JDMF on PharmaCompass.
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