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EUROAPI, the leading small molecules API player, provides both API sales & CDMO services. 
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01 EUROAPI Hungary Ltd. (1)
02 Dipharma Francis S. r. l. (1)
01 Selegiline hydrochloride (2)
01 France (1)
02 Italy (1)
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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 NCGC00024994-06 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NCGC00024994-06, including repackagers and relabelers. The FDA regulates NCGC00024994-06 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NCGC00024994-06 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 NCGC00024994-06 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A NCGC00024994-06 supplier is an individual or a company that provides NCGC00024994-06 active pharmaceutical ingredient (API) or NCGC00024994-06 finished formulations upon request. The NCGC00024994-06 suppliers may include NCGC00024994-06 API manufacturers, exporters, distributors and traders.
click here to find a list of NCGC00024994-06 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 NCGC00024994-06 Drug Master File in Japan (NCGC00024994-06 JDMF) empowers NCGC00024994-06 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 NCGC00024994-06 JDMF during the approval evaluation for pharmaceutical products. At the time of NCGC00024994-06 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 NCGC00024994-06 suppliers with JDMF on PharmaCompass.
