Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
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01 1BIOPHORE INDIA PHARMACEUTICALS PVT. LTD. Hyderabad IN
02 1CHONGQING HUAPONT PHARMACEUTICAL CO., LTD. Chongqing CN
03 1DSM Nutritional Products Ltd. Kaiseraugst CH
04 2OLON S.P.A. Rodano IT
05 1SIEGFRIED PHARMACHEMIKALIEN MINDEN GMBH Minden DE
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01 5Tretinoin
02 1Tretinoin, Type 2
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01 1China
02 1India
03 2Italy
04 1Switzerland
05 1U.S.A
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01 5Valid
02 1Withdrawn by Holder
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
Certificate Number : R0-CEP 2019-124 - Rev 00
Status : Valid
Issue Date : 2021-07-01
Type : Chemical
Substance Number : 693
Certificate Number : R0-CEP 2020-183 - Rev 00
Status : Valid
Issue Date : 2022-09-05
Type : Chemical
Substance Number : 693
Certificate Number : CEP 1998-082 - Rev 08
Status : Valid
Issue Date : 2025-02-24
Type : Chemical
Substance Number : 693
Certificate Number : CEP 2010-034 - Rev 02
Status : Valid
Issue Date : 2025-03-05
Type : Chemical
Substance Number : 693
Certificate Number : R1-CEP 2009-350 - Rev 01
Status : Valid
Issue Date : 2016-04-22
Type : Chemical
Substance Number : 693
Certificate Number : R1-CEP 1996-047 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2007-04-05
Type : Chemical
Substance Number : 693
60
PharmaCompass offers a list of Tretinoin 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 Tretinoin manufacturer or Tretinoin supplier for your needs.
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PharmaCompass also assists you with knowing the Tretinoin API Price utilized in the formulation of products. Tretinoin API Price is not always fixed or binding as the Tretinoin Price is obtained through a variety of data sources. The Tretinoin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cordes vas manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cordes vas, including repackagers and relabelers. The FDA regulates Cordes vas manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cordes vas 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 Cordes vas supplier is an individual or a company that provides Cordes vas active pharmaceutical ingredient (API) or Cordes vas finished formulations upon request. The Cordes vas suppliers may include Cordes vas API manufacturers, exporters, distributors and traders.
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A Cordes vas CEP of the European Pharmacopoeia monograph is often referred to as a Cordes vas Certificate of Suitability (COS). The purpose of a Cordes vas CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cordes vas EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cordes vas to their clients by showing that a Cordes vas CEP has been issued for it. The manufacturer submits a Cordes vas CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cordes vas CEP holder for the record. Additionally, the data presented in the Cordes vas CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cordes vas DMF.
A Cordes vas CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cordes vas 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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We have 4 companies offering Cordes vas
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