TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1TAPI CZECH INDUSTRIES S.R.O. Opava CZ
02 1CURIA ITALY S.R.L. Rozzano, Milano IT
01 2Dihydroergotamine mesilate
01 1Israel
02 1U.S.A
01 2Valid
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 : CEP 2005-107 - Rev 03
Status : Valid
Issue Date : 2025-02-28
Type : Chemical
Substance Number : 551
Certificate Number : R1-CEP 2000-183 - Rev 08
Status : Valid
Issue Date : 2023-03-08
Type : Chemical
Substance Number : 551
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PharmaCompass offers a list of Dihydroergotamine Mesylate 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 Dihydroergotamine Mesylate manufacturer or Dihydroergotamine Mesylate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dihydroergotamine Mesylate manufacturer or Dihydroergotamine Mesylate supplier.
PharmaCompass also assists you with knowing the Dihydroergotamine Mesylate API Price utilized in the formulation of products. Dihydroergotamine Mesylate API Price is not always fixed or binding as the Dihydroergotamine Mesylate Price is obtained through a variety of data sources. The Dihydroergotamine Mesylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Angionorm manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Angionorm, including repackagers and relabelers. The FDA regulates Angionorm manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Angionorm 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 Angionorm manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Angionorm supplier is an individual or a company that provides Angionorm active pharmaceutical ingredient (API) or Angionorm finished formulations upon request. The Angionorm suppliers may include Angionorm API manufacturers, exporters, distributors and traders.
click here to find a list of Angionorm suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Angionorm CEP of the European Pharmacopoeia monograph is often referred to as a Angionorm Certificate of Suitability (COS). The purpose of a Angionorm CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Angionorm EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Angionorm to their clients by showing that a Angionorm CEP has been issued for it. The manufacturer submits a Angionorm CEP (COS) as part of the market authorization procedure, and it takes on the role of a Angionorm CEP holder for the record. Additionally, the data presented in the Angionorm CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Angionorm DMF.
A Angionorm CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Angionorm 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 Angionorm suppliers with CEP (COS) on PharmaCompass.
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