A Myleran, Busulfex, Busulfan CEP of the European Pharmacopoeia monograph is often referred to as a Myleran, Busulfex, Busulfan Certificate of Suitability (COS). The purpose of a Myleran, Busulfex, Busulfan CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Myleran, Busulfex, Busulfan EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Myleran, Busulfex, Busulfan to their clients by showing that a Myleran, Busulfex, Busulfan CEP has been issued for it. The manufacturer submits a Myleran, Busulfex, Busulfan CEP (COS) as part of the market authorization procedure, and it takes on the role of a Myleran, Busulfex, Busulfan CEP holder for the record. Additionally, the data presented in the Myleran, Busulfex, Busulfan CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Myleran, Busulfex, Busulfan DMF.
A Myleran, Busulfex, Busulfan CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Myleran, Busulfex, Busulfan 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 Myleran, Busulfex, Busulfan suppliers with CEP (COS) on PharmaCompass.