Veranova: A CDMO that manages complexity with confidence.
01 1MACFARLAN SMITH LIMITED Edinburgh GB
02 1FRANCOPIA Paris FR
03 1ALCALIBER S.A.U. Madrid ES
04 1S.A.L.A.R.S. S.p.A. Como IT
01 4Morphine hydrochloride trihydrate
01 1France
02 1Spain
03 2U.S.A
01 4Valid
Veranova: A CDMO that manages complexity with confidence.
Veranova: A CDMO that manages complexity with confidence.
Morphine Hydrochloride Trihydrate
Certificate Number : CEP 2001-438 - Rev 08
Status : Valid
Issue Date : 2024-06-20
Type : Chemical
Substance Number : 97
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Morphine Hydrochloride Trihydrate
Certificate Number : CEP 2008-208 - Rev 04
Status : Valid
Issue Date : 2024-04-25
Type : Chemical
Substance Number : 97
Morphine Hydrochloride Trihydrate
Certificate Number : CEP 2007-104 - Rev 03
Status : Valid
Issue Date : 2024-01-23
Type : Chemical
Substance Number : 97
Morphine Hydrochloride Trihydrate
Certificate Number : CEP 2009-339 - Rev 01
Status : Valid
Issue Date : 2024-06-20
Type : Chemical
Substance Number : 97
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A Theba-Intran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Theba-Intran, including repackagers and relabelers. The FDA regulates Theba-Intran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Theba-Intran API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Theba-Intran supplier is an individual or a company that provides Theba-Intran active pharmaceutical ingredient (API) or Theba-Intran finished formulations upon request. The Theba-Intran suppliers may include Theba-Intran API manufacturers, exporters, distributors and traders.
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A Theba-Intran CEP of the European Pharmacopoeia monograph is often referred to as a Theba-Intran Certificate of Suitability (COS). The purpose of a Theba-Intran CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Theba-Intran EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Theba-Intran to their clients by showing that a Theba-Intran CEP has been issued for it. The manufacturer submits a Theba-Intran CEP (COS) as part of the market authorization procedure, and it takes on the role of a Theba-Intran CEP holder for the record. Additionally, the data presented in the Theba-Intran CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Theba-Intran DMF.
A Theba-Intran CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Theba-Intran CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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