A SODIUM CHLORIDE, U.S.P. CEP of the European Pharmacopoeia monograph is often referred to as a SODIUM CHLORIDE, U.S.P. Certificate of Suitability (COS). The purpose of a SODIUM CHLORIDE, U.S.P. CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of SODIUM CHLORIDE, U.S.P. EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of SODIUM CHLORIDE, U.S.P. to their clients by showing that a SODIUM CHLORIDE, U.S.P. CEP has been issued for it. The manufacturer submits a SODIUM CHLORIDE, U.S.P. CEP (COS) as part of the market authorization procedure, and it takes on the role of a SODIUM CHLORIDE, U.S.P. CEP holder for the record. Additionally, the data presented in the SODIUM CHLORIDE, U.S.P. CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the SODIUM CHLORIDE, U.S.P. DMF.
A SODIUM CHLORIDE, U.S.P. CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. SODIUM CHLORIDE, U.S.P. CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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