LEBSA- Your strategic API source for niche molecules.
01 1Laboratorios Espinos Y Bofill S.A. Cornella de Llobregat ES
02 2LABORATORIUM OFICHEM B.V. Ter Apel NL
LEBSA- Your strategic API source for niche molecules.
Certificate Number : CEP 2016-054 - Rev 01
Status : Valid
Issue Date : 2024-12-11
Type : Chemical
Substance Number : 143
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
Certificate Number : R0-CEP 2020-131 - Rev 00
Status : Valid
Issue Date : 2023-01-25
Type : Chemical
Substance Number : 143
Laboratorium Ofichem, offering a flexible, high-tech environment to produce broad range of APIs for Human & Vet pharmaceutical markets.
Histamine Dihydrochloride, Process 1857
Certificate Number : CEP 2024-122 - Rev 00
Status : Valid
Issue Date : 2024-07-02
Type : Chemical
Substance Number : 143
A Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard, including repackagers and relabelers. The FDA regulates Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard 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 Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard supplier is an individual or a company that provides Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard active pharmaceutical ingredient (API) or Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard finished formulations upon request. The Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard suppliers may include Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard API manufacturers, exporters, distributors and traders.
click here to find a list of Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard CEP of the European Pharmacopoeia monograph is often referred to as a Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard Certificate of Suitability (COS). The purpose of a Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard to their clients by showing that a Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard CEP has been issued for it. The manufacturer submits a Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard CEP (COS) as part of the market authorization procedure, and it takes on the role of a Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard CEP holder for the record. Additionally, the data presented in the Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard DMF.
A Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard 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 Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard suppliers with CEP (COS) on PharmaCompass.
We have 2 companies offering Histamine dihydrochloride, United States Pharmacopeia (USP) Reference Standard
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