ICE Pharma offers a unique range of bile acid products and best-in-class services for the pharmaceutical industry.
01 1ICE S.p.A.
02 1New Zealand Pharmaceuticals Ltd.
01 1Cholic Acid Pharma Grade
02 1Sodium Cholate
01 1Italy
02 1New Zealand
ICE Pharma offers a unique range of bile acid products and best-in-class services for the pharmaceutical industry.
Registration Number : 304MF10051
Registrant's Address : Via Sicilia, 8/10 42122 Reggio Emilia, ITALY
Initial Date of Registration : 2022-03-10
Latest Date of Registration : 2023-02-02
Registration Number : 306MF10023
Registrant's Address : 68 Weld Street, RD2 Palmerston North 4472, New Zealand
Initial Date of Registration : 2024-02-07
Latest Date of Registration : 2024-02-07
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PharmaCompass offers a list of Cholic Acid 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 Cholic Acid manufacturer or Cholic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cholic Acid manufacturer or Cholic Acid supplier.
PharmaCompass also assists you with knowing the Cholic Acid API Price utilized in the formulation of products. Cholic Acid API Price is not always fixed or binding as the Cholic Acid Price is obtained through a variety of data sources. The Cholic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E1000 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E1000, including repackagers and relabelers. The FDA regulates E1000 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E1000 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 E1000 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E1000 supplier is an individual or a company that provides E1000 active pharmaceutical ingredient (API) or E1000 finished formulations upon request. The E1000 suppliers may include E1000 API manufacturers, exporters, distributors and traders.
click here to find a list of E1000 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The E1000 Drug Master File in Japan (E1000 JDMF) empowers E1000 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the E1000 JDMF during the approval evaluation for pharmaceutical products. At the time of E1000 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of E1000 suppliers with JDMF on PharmaCompass.
We have 2 companies offering E1000
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