Axplora is your partner of choice for complex APIs.
01 1Farmabios S. p. A.
01 1Fluocinolone Acetonide
01 1Germany
Axplora is your 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 Synalar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Synalar, including repackagers and relabelers. The FDA regulates Synalar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Synalar 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 Synalar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Synalar supplier is an individual or a company that provides Synalar active pharmaceutical ingredient (API) or Synalar finished formulations upon request. The Synalar suppliers may include Synalar API manufacturers, exporters, distributors and traders.
click here to find a list of Synalar 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 Synalar Drug Master File in Japan (Synalar JDMF) empowers Synalar 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 Synalar JDMF during the approval evaluation for pharmaceutical products. At the time of Synalar 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 Synalar suppliers with JDMF on PharmaCompass.
