01 1Baxter Deutschland GmbH
01 1Mesna
01 1U.S.A
Registration Number : 223MF10085
Registrant's Address : Edisonstrasse 4,85716 Unterschleissheim, Germany
Initial Date of Registration : 2011-06-17
Latest Date of Registration : 2011-06-17
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PharmaCompass offers a list of Mesna 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 Mesna manufacturer or Mesna supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mesna manufacturer or Mesna supplier.
PharmaCompass also assists you with knowing the Mesna API Price utilized in the formulation of products. Mesna API Price is not always fixed or binding as the Mesna Price is obtained through a variety of data sources. The Mesna Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mucofluid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mucofluid, including repackagers and relabelers. The FDA regulates Mucofluid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mucofluid 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 Mucofluid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mucofluid supplier is an individual or a company that provides Mucofluid active pharmaceutical ingredient (API) or Mucofluid finished formulations upon request. The Mucofluid suppliers may include Mucofluid API manufacturers, exporters, distributors and traders.
click here to find a list of Mucofluid 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 Mucofluid Drug Master File in Japan (Mucofluid JDMF) empowers Mucofluid 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 Mucofluid JDMF during the approval evaluation for pharmaceutical products. At the time of Mucofluid 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 Mucofluid suppliers with JDMF on PharmaCompass.
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