01 1Dipharma Francis Srl
01 1Masung LS Co., Ltd.
01 1Selegiline hydrochloride
01 1Italy
Registrant Name : Masung LS Co., Ltd.
Registration Date : 2021-08-19
Registration Number : 20210819-209-J-950
Manufacturer Name : Dipharma Francis Srl
Manufacturer Address : Via Bissone 5 20021 Baranzate (MI), Italy
61
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 Jumex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Jumex, including repackagers and relabelers. The FDA regulates Jumex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Jumex 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 Jumex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Jumex supplier is an individual or a company that provides Jumex active pharmaceutical ingredient (API) or Jumex finished formulations upon request. The Jumex suppliers may include Jumex API manufacturers, exporters, distributors and traders.
click here to find a list of Jumex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Jumex Drug Master File in Korea (Jumex KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Jumex. The MFDS reviews the Jumex KDMF as part of the drug registration process and uses the information provided in the Jumex KDMF to evaluate the safety and efficacy of the drug.
After submitting a Jumex KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Jumex API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Jumex suppliers with KDMF on PharmaCompass.
