EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI Hungary Ltd.
02 1Dipharma Francis S. r. l.
01 2Selegiline hydrochloride
01 1France
02 1Italy
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Registration Number : 229MF10114
Registrant's Address : To(´) utca 1-5. , 1045 Budapest, Hungary
Initial Date of Registration : 2017-06-30
Latest Date of Registration : 2017-06-30
Registration Number : 219MF10340
Registrant's Address : Via Bissone, 5, 20021-Baranzate, Milano, Italy
Initial Date of Registration : 2007-11-21
Latest Date of Registration : 2023-06-07
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PharmaCompass offers a list of Selegiline 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 Selegiline Hydrochloride manufacturer or Selegiline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Selegiline Hydrochloride manufacturer or Selegiline Hydrochloride supplier.
PharmaCompass also assists you with knowing the Selegiline Hydrochloride API Price utilized in the formulation of products. Selegiline Hydrochloride API Price is not always fixed or binding as the Selegiline Hydrochloride Price is obtained through a variety of data sources. The Selegiline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Selegiline Base manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Selegiline Base, including repackagers and relabelers. The FDA regulates Selegiline Base manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Selegiline Base 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 Selegiline Base manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Selegiline Base supplier is an individual or a company that provides Selegiline Base active pharmaceutical ingredient (API) or Selegiline Base finished formulations upon request. The Selegiline Base suppliers may include Selegiline Base API manufacturers, exporters, distributors and traders.
click here to find a list of Selegiline Base 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 Selegiline Base Drug Master File in Japan (Selegiline Base JDMF) empowers Selegiline Base 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 Selegiline Base JDMF during the approval evaluation for pharmaceutical products. At the time of Selegiline Base 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 Selegiline Base suppliers with JDMF on PharmaCompass.
