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01 1SOLVAY USA INC. Princeton US
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01 1Nonoxinol 9
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01 1U.S.A
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01 1Valid
Certificate Number : R1-CEP 2007-327 - Rev 01
Status : Valid
Issue Date : 2022-05-04
Type : Chemical
Substance Number : 1454
44
PharmaCompass offers a list of NONOXYNOL-9 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 NONOXYNOL-9 manufacturer or NONOXYNOL-9 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred NONOXYNOL-9 manufacturer or NONOXYNOL-9 supplier.
PharmaCompass also assists you with knowing the NONOXYNOL-9 API Price utilized in the formulation of products. NONOXYNOL-9 API Price is not always fixed or binding as the NONOXYNOL-9 Price is obtained through a variety of data sources. The NONOXYNOL-9 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DELFEN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DELFEN, including repackagers and relabelers. The FDA regulates DELFEN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DELFEN 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 DELFEN manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DELFEN supplier is an individual or a company that provides DELFEN active pharmaceutical ingredient (API) or DELFEN finished formulations upon request. The DELFEN suppliers may include DELFEN API manufacturers, exporters, distributors and traders.
click here to find a list of DELFEN suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DELFEN CEP of the European Pharmacopoeia monograph is often referred to as a DELFEN Certificate of Suitability (COS). The purpose of a DELFEN CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DELFEN EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DELFEN to their clients by showing that a DELFEN CEP has been issued for it. The manufacturer submits a DELFEN CEP (COS) as part of the market authorization procedure, and it takes on the role of a DELFEN CEP holder for the record. Additionally, the data presented in the DELFEN CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DELFEN DMF.
A DELFEN CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DELFEN 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 DELFEN suppliers with CEP (COS) on PharmaCompass.