01 1Cambrex Profarmaco Milano S. r. l.
01 1Sotalol Hydrochloride
01 1U.S.A
Registration Number : 302MF10102
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2020-08-18
Latest Date of Registration : 2021-05-10
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PharmaCompass offers a list of Sotalol Hydrochloride 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 Sotalol Hydrochloride manufacturer or Sotalol Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sotalol Hydrochloride manufacturer or Sotalol Hydrochloride supplier.
PharmaCompass also assists you with knowing the Sotalol Hydrochloride API Price utilized in the formulation of products. Sotalol Hydrochloride API Price is not always fixed or binding as the Sotalol Hydrochloride Price is obtained through a variety of data sources. The Sotalol Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SORINE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SORINE, including repackagers and relabelers. The FDA regulates SORINE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SORINE 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 SORINE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A SORINE supplier is an individual or a company that provides SORINE active pharmaceutical ingredient (API) or SORINE finished formulations upon request. The SORINE suppliers may include SORINE API manufacturers, exporters, distributors and traders.
click here to find a list of SORINE 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 SORINE Drug Master File in Japan (SORINE JDMF) empowers SORINE 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 SORINE JDMF during the approval evaluation for pharmaceutical products. At the time of SORINE 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 SORINE suppliers with JDMF on PharmaCompass.
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