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
A Remifentanil Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Remifentanil Hydrochloride, including repackagers and relabelers. The FDA regulates Remifentanil Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Remifentanil Hydrochloride 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 Remifentanil Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Remifentanil Hydrochloride supplier is an individual or a company that provides Remifentanil Hydrochloride active pharmaceutical ingredient (API) or Remifentanil Hydrochloride finished formulations upon request. The Remifentanil Hydrochloride suppliers may include Remifentanil Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Remifentanil Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Remifentanil Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Remifentanil Hydrochloride Certificate of Suitability (COS). The purpose of a Remifentanil Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Remifentanil Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Remifentanil Hydrochloride to their clients by showing that a Remifentanil Hydrochloride CEP has been issued for it. The manufacturer submits a Remifentanil Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Remifentanil Hydrochloride CEP holder for the record. Additionally, the data presented in the Remifentanil Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Remifentanil Hydrochloride DMF.
A Remifentanil Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Remifentanil Hydrochloride 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 Remifentanil Hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 8 companies offering Remifentanil Hydrochloride
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