01 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 1Sulindac
01 1Italy
Registration Number : 220MF10202
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2008-09-19
Latest Date of Registration : 2022-02-10
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PharmaCompass offers a list of Sulindac 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 Sulindac manufacturer or Sulindac supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sulindac manufacturer or Sulindac supplier.
PharmaCompass also assists you with knowing the Sulindac API Price utilized in the formulation of products. Sulindac API Price is not always fixed or binding as the Sulindac Price is obtained through a variety of data sources. The Sulindac Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gum copal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gum copal, including repackagers and relabelers. The FDA regulates Gum copal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gum copal 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 Gum copal manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gum copal supplier is an individual or a company that provides Gum copal active pharmaceutical ingredient (API) or Gum copal finished formulations upon request. The Gum copal suppliers may include Gum copal API manufacturers, exporters, distributors and traders.
click here to find a list of Gum copal 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 Gum copal Drug Master File in Japan (Gum copal JDMF) empowers Gum copal 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 Gum copal JDMF during the approval evaluation for pharmaceutical products. At the time of Gum copal 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 Gum copal suppliers with JDMF on PharmaCompass.
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