Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab Private Limited
02 1Farmabios S. p. A.
03 1Curia Spain S. A. U.
04 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Registration Number : 229MF10086
Registrant's Address : 385/2, Pigdamber, Off. A. B. Road, Rau, Indore 453331 (M.P.) India
Initial Date of Registration : 2017-04-25
Latest Date of Registration : 2020-10-05
Axplora is your partner of choice for complex APIs.
For manufacturing only Clobetasol propionate
Registration Number : 222MF10130
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2010-04-12
Latest Date of Registration : 2019-04-09
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PharmaCompass offers a list of Clobetasol Propionate 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 Clobetasol Propionate manufacturer or Clobetasol Propionate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clobetasol Propionate manufacturer or Clobetasol Propionate supplier.
PharmaCompass also assists you with knowing the Clobetasol Propionate API Price utilized in the formulation of products. Clobetasol Propionate API Price is not always fixed or binding as the Clobetasol Propionate Price is obtained through a variety of data sources. The Clobetasol Propionate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A OLUX FOAM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of OLUX FOAM, including repackagers and relabelers. The FDA regulates OLUX FOAM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. OLUX FOAM API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A OLUX FOAM supplier is an individual or a company that provides OLUX FOAM active pharmaceutical ingredient (API) or OLUX FOAM finished formulations upon request. The OLUX FOAM suppliers may include OLUX FOAM API manufacturers, exporters, distributors and traders.
click here to find a list of OLUX FOAM 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 OLUX FOAM Drug Master File in Japan (OLUX FOAM JDMF) empowers OLUX FOAM 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 OLUX FOAM JDMF during the approval evaluation for pharmaceutical products. At the time of OLUX FOAM 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 OLUX FOAM suppliers with JDMF on PharmaCompass.
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