TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TEVA CZECH INDUSTRIES S.R.O. Opava CZ
01 1Methylergometrine maleate
01 1Israel
01 1Valid
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
Certificate Number : R1-CEP 2012-405 - Rev 01
Status : Valid
Issue Date : 2022-09-12
Type : Chemical
Substance Number : 1788
A Methylergonovine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methylergonovine, including repackagers and relabelers. The FDA regulates Methylergonovine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methylergonovine 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 Methylergonovine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Methylergonovine supplier is an individual or a company that provides Methylergonovine active pharmaceutical ingredient (API) or Methylergonovine finished formulations upon request. The Methylergonovine suppliers may include Methylergonovine API manufacturers, exporters, distributors and traders.
click here to find a list of Methylergonovine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Methylergonovine CEP of the European Pharmacopoeia monograph is often referred to as a Methylergonovine Certificate of Suitability (COS). The purpose of a Methylergonovine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Methylergonovine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Methylergonovine to their clients by showing that a Methylergonovine CEP has been issued for it. The manufacturer submits a Methylergonovine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Methylergonovine CEP holder for the record. Additionally, the data presented in the Methylergonovine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Methylergonovine DMF.
A Methylergonovine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Methylergonovine 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 Methylergonovine suppliers with CEP (COS) on PharmaCompass.
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