Axplora- The partner of choice for complex APIs.
01 1Farmabios S. p. A.
01 1Fluocinolone Acetonide
01 1Germany
Axplora- The partner of choice for complex APIs.
Registration Number : 218MF10445
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2010-03-17
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PharmaCompass offers a list of Fluocinolone Acetonide 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 Fluocinolone Acetonide manufacturer or Fluocinolone Acetonide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluocinolone Acetonide manufacturer or Fluocinolone Acetonide supplier.
PharmaCompass also assists you with knowing the Fluocinolone Acetonide API Price utilized in the formulation of products. Fluocinolone Acetonide API Price is not always fixed or binding as the Fluocinolone Acetonide Price is obtained through a variety of data sources. The Fluocinolone Acetonide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gelidina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gelidina, including repackagers and relabelers. The FDA regulates Gelidina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gelidina 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 Gelidina manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gelidina supplier is an individual or a company that provides Gelidina active pharmaceutical ingredient (API) or Gelidina finished formulations upon request. The Gelidina suppliers may include Gelidina API manufacturers, exporters, distributors and traders.
click here to find a list of Gelidina 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 Gelidina Drug Master File in Japan (Gelidina JDMF) empowers Gelidina 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 Gelidina JDMF during the approval evaluation for pharmaceutical products. At the time of Gelidina 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 Gelidina suppliers with JDMF on PharmaCompass.
