Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
01 1MINAKEM Dunkerque FR
02 1MACFARLAN SMITH LIMITED Edinburgh GB
03 1Fine Chemicals Corporation (Pty) Ltd. Goodwood ZA
04 1AREVIPHARMA GMBH Radebeul DE
05 1CILAG AG Schaffhausen CH
06 1HAMELN RDS S.R.O. Modra SK
07 1Kern Pharma, S.L. Terrassa ES
08 1YICHANG HUMANWELL PHARMACEUTICAL CO., LTD. Yichang CN
Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
Certificate Number : R0-CEP 2020-323 - Rev 00
Status : Valid
Issue Date : 2022-03-14
Type : Chemical
Substance Number : 2644
Veranova: A CDMO that manages complexity with confidence.
Certificate Number : CEP 2018-137 - Rev 01
Status : Valid
Issue Date : 2024-08-06
Type : Chemical
Substance Number : 2644
Certificate Number : CEP 2018-240 - Rev 03
Status : Valid
Issue Date : 2024-06-28
Type : Chemical
Substance Number : 2644
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PharmaCompass offers a list of Remifentanil 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 Remifentanil manufacturer or Remifentanil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Remifentanil manufacturer or Remifentanil supplier.
PharmaCompass also assists you with knowing the Remifentanil API Price utilized in the formulation of products. Remifentanil API Price is not always fixed or binding as the Remifentanil Price is obtained through a variety of data sources. The Remifentanil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ultiva manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ultiva, including repackagers and relabelers. The FDA regulates Ultiva manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ultiva 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 Ultiva manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ultiva supplier is an individual or a company that provides Ultiva active pharmaceutical ingredient (API) or Ultiva finished formulations upon request. The Ultiva suppliers may include Ultiva API manufacturers, exporters, distributors and traders.
click here to find a list of Ultiva suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ultiva CEP of the European Pharmacopoeia monograph is often referred to as a Ultiva Certificate of Suitability (COS). The purpose of a Ultiva CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ultiva EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ultiva to their clients by showing that a Ultiva CEP has been issued for it. The manufacturer submits a Ultiva CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ultiva CEP holder for the record. Additionally, the data presented in the Ultiva CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ultiva DMF.
A Ultiva CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ultiva 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 Ultiva suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering Ultiva
Get in contact with the supplier of your choice:
