01 1CHINESE PEPTIDE COMPANY Hangzhou CN
02 1HYBIO PHARMACEUTICAL CO., LTD. Shenzhen CN
03 1PIRAMAL PHARMA LIMITED Mumbai IN
04 1PolyPeptide Laboratories (Sweden) AB Limhamn SE
01 4Terlipressin
01 2China
02 2U.S.A
01 4Valid
Certificate Number : R0-CEP 2020-111 - Rev 00
Status : Valid
Issue Date : 2022-05-23
Type : Chemical
Substance Number : 2646
Certificate Number : R0-CEP 2020-319 - Rev 00
Status : Valid
Issue Date : 2021-10-28
Type : Chemical
Substance Number : 2646
Certificate Number : R0-CEP 2021-470 - Rev 00
Status : Valid
Issue Date : 2022-12-06
Type : Chemical
Substance Number : 2646
Certificate Number : R0-CEP 2019-316 - Rev 00
Status : Valid
Issue Date : 2021-05-21
Type : Chemical
Substance Number : 2646
A Terlipressin Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Terlipressin Acetate, including repackagers and relabelers. The FDA regulates Terlipressin Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Terlipressin Acetate 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 Terlipressin Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Terlipressin Acetate supplier is an individual or a company that provides Terlipressin Acetate active pharmaceutical ingredient (API) or Terlipressin Acetate finished formulations upon request. The Terlipressin Acetate suppliers may include Terlipressin Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Terlipressin Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Terlipressin Acetate CEP of the European Pharmacopoeia monograph is often referred to as a Terlipressin Acetate Certificate of Suitability (COS). The purpose of a Terlipressin Acetate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Terlipressin Acetate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Terlipressin Acetate to their clients by showing that a Terlipressin Acetate CEP has been issued for it. The manufacturer submits a Terlipressin Acetate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Terlipressin Acetate CEP holder for the record. Additionally, the data presented in the Terlipressin Acetate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Terlipressin Acetate DMF.
A Terlipressin Acetate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Terlipressin Acetate 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 Terlipressin Acetate suppliers with CEP (COS) on PharmaCompass.
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