TAPI offers customized CDMO Solutions for API development and manufacturing services.
01 1TEVA CZECH INDUSTRIES S.R.O. Opava CZ
01 1Codergocrine mesilate
01 1Israel
01 1Valid
TAPI offers customized CDMO Solutions for API development and manufacturing services.
TAPI offers customized CDMO Solutions for API development and manufacturing services.
Certificate Number : R1-CEP 2009-143 - Rev 02
Status : Valid
Issue Date : 2023-04-14
Type : Chemical
Substance Number : 2060
A Co-Dergocrine Mesilate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Co-Dergocrine Mesilate, including repackagers and relabelers. The FDA regulates Co-Dergocrine Mesilate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Co-Dergocrine Mesilate 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 Co-Dergocrine Mesilate supplier is an individual or a company that provides Co-Dergocrine Mesilate active pharmaceutical ingredient (API) or Co-Dergocrine Mesilate finished formulations upon request. The Co-Dergocrine Mesilate suppliers may include Co-Dergocrine Mesilate API manufacturers, exporters, distributors and traders.
click here to find a list of Co-Dergocrine Mesilate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Co-Dergocrine Mesilate CEP of the European Pharmacopoeia monograph is often referred to as a Co-Dergocrine Mesilate Certificate of Suitability (COS). The purpose of a Co-Dergocrine Mesilate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Co-Dergocrine Mesilate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Co-Dergocrine Mesilate to their clients by showing that a Co-Dergocrine Mesilate CEP has been issued for it. The manufacturer submits a Co-Dergocrine Mesilate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Co-Dergocrine Mesilate CEP holder for the record. Additionally, the data presented in the Co-Dergocrine Mesilate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Co-Dergocrine Mesilate DMF.
A Co-Dergocrine Mesilate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Co-Dergocrine Mesilate 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 Co-Dergocrine Mesilate suppliers with CEP (COS) on PharmaCompass.
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