01 1dsm-firmenich Switzerland AG
01 1Dry vitamin A acetate, type 500B Dry Vitamin A A cetate 500B①
01 1Netherlands
Dry Vitamin A Acetate, Type 500B ①
Registration Number : 224MF10063
Registrant's Address : Wurmisweg 576 4303 Kaiseraugst
Initial Date of Registration : 2012-04-01
Latest Date of Registration : 2012-04-01
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PharmaCompass offers a list of Vitamin A Acetate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Vitamin A Acetate manufacturer or Vitamin A Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin A Acetate manufacturer or Vitamin A Acetate supplier.
A Vitamin A1 acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vitamin A1 acetate, including repackagers and relabelers. The FDA regulates Vitamin A1 acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vitamin A1 acetate 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 Vitamin A1 acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Vitamin A1 acetate supplier is an individual or a company that provides Vitamin A1 acetate active pharmaceutical ingredient (API) or Vitamin A1 acetate finished formulations upon request. The Vitamin A1 acetate suppliers may include Vitamin A1 acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Vitamin A1 acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Vitamin A1 acetate Drug Master File in Japan (Vitamin A1 acetate JDMF) empowers Vitamin A1 acetate 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 Vitamin A1 acetate JDMF during the approval evaluation for pharmaceutical products. At the time of Vitamin A1 acetate 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 Vitamin A1 acetate suppliers with JDMF on PharmaCompass.
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