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01 1PharmaZell GmbH Raubling DE
02 1Bretagne Chimie Fine Pleucadeuc FR
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01 2Cystine
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01 1France
02 1Germany
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01 2Valid
Certificate Number : R1-CEP 2002-037 - Rev 02
Status : Valid
Issue Date : 2017-01-23
Type : Chemical
Substance Number : 998
Certificate Number : CEP 2023-272 - Rev 00
Status : Valid
Issue Date : 2024-09-02
Type : Chemical
Substance Number : 998
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PharmaCompass offers a list of Cystine 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 Cystine manufacturer or Cystine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cystine manufacturer or Cystine supplier.
PharmaCompass also assists you with knowing the Cystine API Price utilized in the formulation of products. Cystine API Price is not always fixed or binding as the Cystine Price is obtained through a variety of data sources. The Cystine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ACETYLCYSTEINE IMPURITY A (L-CYSTINE) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ACETYLCYSTEINE IMPURITY A (L-CYSTINE), including repackagers and relabelers. The FDA regulates ACETYLCYSTEINE IMPURITY A (L-CYSTINE) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ACETYLCYSTEINE IMPURITY A (L-CYSTINE) 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 ACETYLCYSTEINE IMPURITY A (L-CYSTINE) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ACETYLCYSTEINE IMPURITY A (L-CYSTINE) supplier is an individual or a company that provides ACETYLCYSTEINE IMPURITY A (L-CYSTINE) active pharmaceutical ingredient (API) or ACETYLCYSTEINE IMPURITY A (L-CYSTINE) finished formulations upon request. The ACETYLCYSTEINE IMPURITY A (L-CYSTINE) suppliers may include ACETYLCYSTEINE IMPURITY A (L-CYSTINE) API manufacturers, exporters, distributors and traders.
click here to find a list of ACETYLCYSTEINE IMPURITY A (L-CYSTINE) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A ACETYLCYSTEINE IMPURITY A (L-CYSTINE) CEP of the European Pharmacopoeia monograph is often referred to as a ACETYLCYSTEINE IMPURITY A (L-CYSTINE) Certificate of Suitability (COS). The purpose of a ACETYLCYSTEINE IMPURITY A (L-CYSTINE) CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of ACETYLCYSTEINE IMPURITY A (L-CYSTINE) EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of ACETYLCYSTEINE IMPURITY A (L-CYSTINE) to their clients by showing that a ACETYLCYSTEINE IMPURITY A (L-CYSTINE) CEP has been issued for it. The manufacturer submits a ACETYLCYSTEINE IMPURITY A (L-CYSTINE) CEP (COS) as part of the market authorization procedure, and it takes on the role of a ACETYLCYSTEINE IMPURITY A (L-CYSTINE) CEP holder for the record. Additionally, the data presented in the ACETYLCYSTEINE IMPURITY A (L-CYSTINE) CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the ACETYLCYSTEINE IMPURITY A (L-CYSTINE) DMF.
A ACETYLCYSTEINE IMPURITY A (L-CYSTINE) CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. ACETYLCYSTEINE IMPURITY A (L-CYSTINE) 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 ACETYLCYSTEINE IMPURITY A (L-CYSTINE) suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering ACETYLCYSTEINE IMPURITY A (L-CYSTINE)
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