Veranova: A CDMO that manages complexity with confidence.
01 1MACFARLAN SMITH LIMITED Edinburgh GB
02 1NORAMCO, LLC. Wilmington US
03 1AREVIPHARMA GMBH Radebeul DE
04 1CHR. OLESEN SYNTHESIS A/S Hvidovre DK
05 1MINAKEM HIGH POTENT Mont-Saint-Guibert BE
06 1SANECA PHARMACEUTICALS A.S. Hlohovec SK
07 1SIEGFRIED LTD. Zofingen CH
08 1YICHANG HUMANWELL PHARMACEUTICAL CO., LTD. Yichang CN
Veranova: A CDMO that manages complexity with confidence.
Certificate Number : R1-CEP 2004-265 - Rev 02
Status : Valid
Issue Date : 2017-02-27
Type : Chemical
Substance Number : 2099
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
Certificate Number : R1-CEP 2006-169 - Rev 04
Status : Valid
Issue Date : 2021-03-25
Type : Chemical
Substance Number : 2099
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PharmaCompass offers a list of Hydromorphone 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 Hydromorphone Hydrochloride manufacturer or Hydromorphone Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydromorphone Hydrochloride manufacturer or Hydromorphone Hydrochloride supplier.
PharmaCompass also assists you with knowing the Hydromorphone Hydrochloride API Price utilized in the formulation of products. Hydromorphone Hydrochloride API Price is not always fixed or binding as the Hydromorphone Hydrochloride Price is obtained through a variety of data sources. The Hydromorphone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hydromorphon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydromorphon, including repackagers and relabelers. The FDA regulates Hydromorphon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydromorphon 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 Hydromorphon manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydromorphon supplier is an individual or a company that provides Hydromorphon active pharmaceutical ingredient (API) or Hydromorphon finished formulations upon request. The Hydromorphon suppliers may include Hydromorphon API manufacturers, exporters, distributors and traders.
click here to find a list of Hydromorphon suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Hydromorphon CEP of the European Pharmacopoeia monograph is often referred to as a Hydromorphon Certificate of Suitability (COS). The purpose of a Hydromorphon CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Hydromorphon EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Hydromorphon to their clients by showing that a Hydromorphon CEP has been issued for it. The manufacturer submits a Hydromorphon CEP (COS) as part of the market authorization procedure, and it takes on the role of a Hydromorphon CEP holder for the record. Additionally, the data presented in the Hydromorphon CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Hydromorphon DMF.
A Hydromorphon CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Hydromorphon 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 Hydromorphon suppliers with CEP (COS) on PharmaCompass.
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