Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
01 1Medichem, S.A. Sant Joan Despí ES
01 1Chlorhexidine diacetate
01 1Spain
01 1Valid
Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
Certificate Number : CEP 2018-123 - Rev 02
Status : Valid
Issue Date : 2024-02-19
Type : Chemical
Substance Number : 657
A Chlorhexidine Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorhexidine Acetate, including repackagers and relabelers. The FDA regulates Chlorhexidine Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorhexidine Acetate 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 Chlorhexidine Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Chlorhexidine Acetate supplier is an individual or a company that provides Chlorhexidine Acetate active pharmaceutical ingredient (API) or Chlorhexidine Acetate finished formulations upon request. The Chlorhexidine Acetate suppliers may include Chlorhexidine Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorhexidine Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Chlorhexidine Acetate CEP of the European Pharmacopoeia monograph is often referred to as a Chlorhexidine Acetate Certificate of Suitability (COS). The purpose of a Chlorhexidine Acetate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Chlorhexidine Acetate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Chlorhexidine Acetate to their clients by showing that a Chlorhexidine Acetate CEP has been issued for it. The manufacturer submits a Chlorhexidine Acetate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Chlorhexidine Acetate CEP holder for the record. Additionally, the data presented in the Chlorhexidine Acetate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Chlorhexidine Acetate DMF.
A Chlorhexidine Acetate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Chlorhexidine Acetate 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 Chlorhexidine Acetate suppliers with CEP (COS) on PharmaCompass.
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