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
A Cholic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cholic Acid, including repackagers and relabelers. The FDA regulates Cholic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cholic Acid 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 Cholic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cholic Acid supplier is an individual or a company that provides Cholic Acid active pharmaceutical ingredient (API) or Cholic Acid finished formulations upon request. The Cholic Acid suppliers may include Cholic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Cholic Acid 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 Cholic Acid Drug Master File in Japan (Cholic Acid JDMF) empowers Cholic Acid 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 Cholic Acid JDMF during the approval evaluation for pharmaceutical products. At the time of Cholic Acid 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 Cholic Acid suppliers with JDMF on PharmaCompass.
We have 2 companies offering Cholic Acid
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
