Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
01 1Farmhispania, S.A. Montmeló ES
02 2Chunghwa Chemical Synthesis & Biotech Co., Ltd. Shu-Lin TW
03 4BIOCON LIMITED Bengaluru IN
04 1BRIGHTGENE BIO-MEDICAL TECHNOLOGY CO., LTD. Suzhou CN
05 1CKD BIO CORPORATION Sapgyo-eup KR
06 1CONCORD BIOTECH LIMITED Ahmedabad IN
07 1SYNTHON B.V. Nijmegen NL
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
Certificate Number : R0-CEP 2019-256 - Rev 02
Status : Valid
Issue Date : 2023-04-27
Type : Chemical
Substance Number : 2918
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Everolimus, With Antioxidant Butylhydroxytoluene...
Certificate Number : CEP 2021-192 - Rev 02
Status : Valid
Issue Date : 2024-02-22
Type : Chemical
Substance Number : 2918
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
Certificate Number : R0-CEP 2020-367 - Rev 01
Status : Valid
Issue Date : 2023-05-16
Type : Chemical
Substance Number : 2918
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PharmaCompass offers a list of Everolimus 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 Everolimus manufacturer or Everolimus supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Everolimus manufacturer or Everolimus supplier.
PharmaCompass also assists you with knowing the Everolimus API Price utilized in the formulation of products. Everolimus API Price is not always fixed or binding as the Everolimus Price is obtained through a variety of data sources. The Everolimus Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A RAD manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RAD, including repackagers and relabelers. The FDA regulates RAD manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RAD 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 RAD manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A RAD supplier is an individual or a company that provides RAD active pharmaceutical ingredient (API) or RAD finished formulations upon request. The RAD suppliers may include RAD API manufacturers, exporters, distributors and traders.
click here to find a list of RAD suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A RAD CEP of the European Pharmacopoeia monograph is often referred to as a RAD Certificate of Suitability (COS). The purpose of a RAD CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of RAD EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of RAD to their clients by showing that a RAD CEP has been issued for it. The manufacturer submits a RAD CEP (COS) as part of the market authorization procedure, and it takes on the role of a RAD CEP holder for the record. Additionally, the data presented in the RAD CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the RAD DMF.
A RAD CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. RAD 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 RAD suppliers with CEP (COS) on PharmaCompass.
We have 7 companies offering RAD
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