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01 1XELLIA PHARMACEUTICALS LTD Budapest HU
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01 1Gramicidin
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01 1Denmark
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01 1Valid
Certificate Number : R1-CEP 2006-132 - Rev 06
Status : Valid
Issue Date : 2018-12-18
Type : Chemical
Substance Number : 907
49
PharmaCompass offers a list of Gramicidin 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 Gramicidin manufacturer or Gramicidin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gramicidin manufacturer or Gramicidin supplier.
PharmaCompass also assists you with knowing the Gramicidin API Price utilized in the formulation of products. Gramicidin API Price is not always fixed or binding as the Gramicidin Price is obtained through a variety of data sources. The Gramicidin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NEOSPORIN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NEOSPORIN, including repackagers and relabelers. The FDA regulates NEOSPORIN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NEOSPORIN 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 NEOSPORIN manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A NEOSPORIN supplier is an individual or a company that provides NEOSPORIN active pharmaceutical ingredient (API) or NEOSPORIN finished formulations upon request. The NEOSPORIN suppliers may include NEOSPORIN API manufacturers, exporters, distributors and traders.
click here to find a list of NEOSPORIN suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A NEOSPORIN CEP of the European Pharmacopoeia monograph is often referred to as a NEOSPORIN Certificate of Suitability (COS). The purpose of a NEOSPORIN CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of NEOSPORIN EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of NEOSPORIN to their clients by showing that a NEOSPORIN CEP has been issued for it. The manufacturer submits a NEOSPORIN CEP (COS) as part of the market authorization procedure, and it takes on the role of a NEOSPORIN CEP holder for the record. Additionally, the data presented in the NEOSPORIN CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the NEOSPORIN DMF.
A NEOSPORIN CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. NEOSPORIN CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of NEOSPORIN suppliers with CEP (COS) on PharmaCompass.
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