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01 1EUROAPI FRANCE
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01 1Methyl succinate
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01 1France
Registration Number : 220MF10128
Registrant's Address : 82 Avenue Raspail 94250 Gentilly France
Initial Date of Registration : 2008-05-15
Latest Date of Registration : 2019-03-05
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PharmaCompass offers a list of Methylprednisolone Hemisuccinate 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 Methylprednisolone Hemisuccinate manufacturer or Methylprednisolone Hemisuccinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methylprednisolone Hemisuccinate manufacturer or Methylprednisolone Hemisuccinate supplier.
PharmaCompass also assists you with knowing the Methylprednisolone Hemisuccinate API Price utilized in the formulation of products. Methylprednisolone Hemisuccinate API Price is not always fixed or binding as the Methylprednisolone Hemisuccinate Price is obtained through a variety of data sources. The Methylprednisolone Hemisuccinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A METHYLPREDNISOLOME HEMISUCCINATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of METHYLPREDNISOLOME HEMISUCCINATE, including repackagers and relabelers. The FDA regulates METHYLPREDNISOLOME HEMISUCCINATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. METHYLPREDNISOLOME HEMISUCCINATE 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 METHYLPREDNISOLOME HEMISUCCINATE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A METHYLPREDNISOLOME HEMISUCCINATE supplier is an individual or a company that provides METHYLPREDNISOLOME HEMISUCCINATE active pharmaceutical ingredient (API) or METHYLPREDNISOLOME HEMISUCCINATE finished formulations upon request. The METHYLPREDNISOLOME HEMISUCCINATE suppliers may include METHYLPREDNISOLOME HEMISUCCINATE API manufacturers, exporters, distributors and traders.
click here to find a list of METHYLPREDNISOLOME HEMISUCCINATE 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 METHYLPREDNISOLOME HEMISUCCINATE Drug Master File in Japan (METHYLPREDNISOLOME HEMISUCCINATE JDMF) empowers METHYLPREDNISOLOME HEMISUCCINATE 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 METHYLPREDNISOLOME HEMISUCCINATE JDMF during the approval evaluation for pharmaceutical products. At the time of METHYLPREDNISOLOME HEMISUCCINATE 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 METHYLPREDNISOLOME HEMISUCCINATE suppliers with JDMF on PharmaCompass.
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