Inke S.A: APIs manufacturing plant.
01 1Inke, S.A. Castellbisbal ES
02 1WAVELENGTH ENTERPRISES LTD. Petah Tikva IL
03 1CIPLA LIMITED Mumbai IN
04 1Chongqing Carelife Pharmaceutical Co. Ltd. Chongqing CN
05 1HUBEI BIOCAUSE HEILEN PHARMACEUTICAL CO., LTD. Jingmen City CN
06 1HUBEI HAOSUN PHARMACEUTICAL CO., LTD. Ezhou CN
07 1ORBION PHARMACEUTICALS PRIVATE LIMITED Irungattukottai IN
08 1ORCHID PHARMA LIMITED Chennai IN
09 1QILU PHARMACEUTICAL CO., LTD. Jinan CN
10 1SCINOPHARM TAIWAN, LTD. Shan-Hua TW
11 1TARO PHARMACEUTICAL INDUSTRIES, LTD. Haifa Bay IL
12 1Zhejiang Hisun Pharmaceutical Co., Ltd. Taizhou City CN
Inke S.A: APIs manufacturing plant.
Certificate Number : R1-CEP 2008-030 - Rev 01
Status : Valid
Issue Date : 2016-03-17
Type : Chemical
Substance Number : 1695
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Certificate Number : CEP 2007-217 - Rev 05
Status : Valid
Issue Date : 2024-10-23
Type : Chemical
Substance Number : 1695
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PharmaCompass offers a list of Granisetron Hydrochloride 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 Granisetron Hydrochloride manufacturer or Granisetron Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Granisetron Hydrochloride manufacturer or Granisetron Hydrochloride supplier.
PharmaCompass also assists you with knowing the Granisetron Hydrochloride API Price utilized in the formulation of products. Granisetron Hydrochloride API Price is not always fixed or binding as the Granisetron Hydrochloride Price is obtained through a variety of data sources. The Granisetron Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AC-478 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AC-478, including repackagers and relabelers. The FDA regulates AC-478 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AC-478 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 AC-478 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AC-478 supplier is an individual or a company that provides AC-478 active pharmaceutical ingredient (API) or AC-478 finished formulations upon request. The AC-478 suppliers may include AC-478 API manufacturers, exporters, distributors and traders.
click here to find a list of AC-478 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A AC-478 CEP of the European Pharmacopoeia monograph is often referred to as a AC-478 Certificate of Suitability (COS). The purpose of a AC-478 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of AC-478 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of AC-478 to their clients by showing that a AC-478 CEP has been issued for it. The manufacturer submits a AC-478 CEP (COS) as part of the market authorization procedure, and it takes on the role of a AC-478 CEP holder for the record. Additionally, the data presented in the AC-478 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the AC-478 DMF.
A AC-478 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. AC-478 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 AC-478 suppliers with CEP (COS) on PharmaCompass.
We have 12 companies offering AC-478
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