Veranova: A CDMO that manages complexity with confidence.
01 1MACFARLAN SMITH LIMITED Edinburgh GB
02 1FRANCOPIA Paris FR
03 3NORAMCO, LLC. Wilmington US
04 1ALKALOIDA CHEMICAL COMPANY ZRT. Tiszavasvari HU
05 1AREVIPHARMA GMBH Radebeul DE
06 1S.A.L.A.R.S. S.p.A. Como IT
07 1SANECA PHARMACEUTICALS A.S. Hlohovec SK
08 2SIEGFRIED LTD. Zofingen CH
09 1SPECGX LLC Webster Groves US
Veranova: A CDMO that manages complexity with confidence.
Certificate Number : CEP 2005-036 - Rev 04
Status : Valid
Issue Date : 2024-04-10
Type : Chemical
Substance Number : 1793
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Certificate Number : CEP 2008-249 - Rev 03
Status : Valid
Issue Date : 2024-03-01
Type : Chemical
Substance Number : 1793
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
Certificate Number : R1-CEP 2011-284 - Rev 02
Status : Valid
Issue Date : 2021-02-24
Type : Chemical
Substance Number : 1793
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
Certificate Number : R1-CEP 2009-058 - Rev 04
Status : Valid
Issue Date : 2022-05-12
Type : Chemical
Substance Number : 1793
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PharmaCompass offers a list of Oxycodone Hydrochloride 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 Oxycodone Hydrochloride manufacturer or Oxycodone Hydrochloride supplier for your needs.
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A Oxygesic manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxygesic, including repackagers and relabelers. The FDA regulates Oxygesic manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxygesic 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 Oxygesic supplier is an individual or a company that provides Oxygesic active pharmaceutical ingredient (API) or Oxygesic finished formulations upon request. The Oxygesic suppliers may include Oxygesic API manufacturers, exporters, distributors and traders.
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A Oxygesic CEP of the European Pharmacopoeia monograph is often referred to as a Oxygesic Certificate of Suitability (COS). The purpose of a Oxygesic CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Oxygesic EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Oxygesic to their clients by showing that a Oxygesic CEP has been issued for it. The manufacturer submits a Oxygesic CEP (COS) as part of the market authorization procedure, and it takes on the role of a Oxygesic CEP holder for the record. Additionally, the data presented in the Oxygesic CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Oxygesic DMF.
A Oxygesic CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Oxygesic 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 Oxygesic suppliers with CEP (COS) on PharmaCompass.
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