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01 1Pharmacia & Upjohn Company Kalamazoo US
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01 1Betamethyl Epoxide, 11 DB, (17a,21-dihydroxy-16b-methyl-9b,11b-oxidopregna-1,4-diene-3,20-dione)
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01 1U.S.A
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01 1Expired
Betamethyl Epoxide, 11 DB, (17a,21-dihydroxy-16b...
Certificate Number : R0-CEP 2001-070 - Rev 00
Status : Expired
Issue Date : 2002-03-04
Type : TSE
Substance Number :
68
PharmaCompass offers a list of Betamethyl Epoxide 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 Betamethyl Epoxide manufacturer or Betamethyl Epoxide supplier for your needs.
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A BETAMETHASONE IMPURITY E [EP IMPURITY] manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BETAMETHASONE IMPURITY E [EP IMPURITY], including repackagers and relabelers. The FDA regulates BETAMETHASONE IMPURITY E [EP IMPURITY] manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BETAMETHASONE IMPURITY E [EP IMPURITY] API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A BETAMETHASONE IMPURITY E [EP IMPURITY] supplier is an individual or a company that provides BETAMETHASONE IMPURITY E [EP IMPURITY] active pharmaceutical ingredient (API) or BETAMETHASONE IMPURITY E [EP IMPURITY] finished formulations upon request. The BETAMETHASONE IMPURITY E [EP IMPURITY] suppliers may include BETAMETHASONE IMPURITY E [EP IMPURITY] API manufacturers, exporters, distributors and traders.
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A BETAMETHASONE IMPURITY E [EP IMPURITY] CEP of the European Pharmacopoeia monograph is often referred to as a BETAMETHASONE IMPURITY E [EP IMPURITY] Certificate of Suitability (COS). The purpose of a BETAMETHASONE IMPURITY E [EP IMPURITY] CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of BETAMETHASONE IMPURITY E [EP IMPURITY] EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of BETAMETHASONE IMPURITY E [EP IMPURITY] to their clients by showing that a BETAMETHASONE IMPURITY E [EP IMPURITY] CEP has been issued for it. The manufacturer submits a BETAMETHASONE IMPURITY E [EP IMPURITY] CEP (COS) as part of the market authorization procedure, and it takes on the role of a BETAMETHASONE IMPURITY E [EP IMPURITY] CEP holder for the record. Additionally, the data presented in the BETAMETHASONE IMPURITY E [EP IMPURITY] CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the BETAMETHASONE IMPURITY E [EP IMPURITY] DMF.
A BETAMETHASONE IMPURITY E [EP IMPURITY] CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. BETAMETHASONE IMPURITY E [EP IMPURITY] 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 BETAMETHASONE IMPURITY E [EP IMPURITY] suppliers with CEP (COS) on PharmaCompass.
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