EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI UK Limited
02 1Ami Lifesciences Private Limited
03 1Apitoria Pharma Private Limited Unit-IV
04 2Formosa Laboratories, Inc.
05 1Shandong Xinhua Pharmaceutical Co.,Ltd
06 7Solara Active Pharma Sciences Limited
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registrant Name : Sanofi-Aventis Korea Co., Ltd.
Registration Date : 2022-10-18
Registration Number : 20221018-209-J-1383
Manufacturer Name : EUROAPI UK Limited
Manufacturer Address : 37 Hollands Road, Haverhill, CB9 8PU, United kingdom
AMI Lifesciences is Driven by Chemistry. Powered by People.
Registrant Name : Leaders Bio Co., Ltd.
Registration Date : 2024-10-25
Registration Number : 20241025-209-J-1648
Manufacturer Name : Ami Lifesciences Private Lim...
Manufacturer Address : Block No. 82/B, ECP Road At & Post. Karakhadi, Tal-Padra, City : Karakhadi-391450, Di...
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PharmaCompass offers a list of Sevelamer Carbonate 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 Sevelamer Carbonate manufacturer or Sevelamer Carbonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sevelamer Carbonate manufacturer or Sevelamer Carbonate supplier.
PharmaCompass also assists you with knowing the Sevelamer Carbonate API Price utilized in the formulation of products. Sevelamer Carbonate API Price is not always fixed or binding as the Sevelamer Carbonate Price is obtained through a variety of data sources. The Sevelamer Carbonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A RENVELA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RENVELA, including repackagers and relabelers. The FDA regulates RENVELA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RENVELA 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 RENVELA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A RENVELA supplier is an individual or a company that provides RENVELA active pharmaceutical ingredient (API) or RENVELA finished formulations upon request. The RENVELA suppliers may include RENVELA API manufacturers, exporters, distributors and traders.
click here to find a list of RENVELA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a RENVELA Drug Master File in Korea (RENVELA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of RENVELA. The MFDS reviews the RENVELA KDMF as part of the drug registration process and uses the information provided in the RENVELA KDMF to evaluate the safety and efficacy of the drug.
After submitting a RENVELA KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their RENVELA API can apply through the Korea Drug Master File (KDMF).
click here to find a list of RENVELA suppliers with KDMF on PharmaCompass.
We have 6 companies offering RENVELA
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