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PharmaCompass offers a list of Lurasidone 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 Lurasidone manufacturer or Lurasidone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lurasidone manufacturer or Lurasidone supplier.
PharmaCompass also assists you with knowing the Lurasidone API Price utilized in the formulation of products. Lurasidone API Price is not always fixed or binding as the Lurasidone Price is obtained through a variety of data sources. The Lurasidone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lurasidone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lurasidone Hydrochloride, including repackagers and relabelers. The FDA regulates Lurasidone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lurasidone Hydrochloride 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 Lurasidone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lurasidone Hydrochloride supplier is an individual or a company that provides Lurasidone Hydrochloride active pharmaceutical ingredient (API) or Lurasidone Hydrochloride finished formulations upon request. The Lurasidone Hydrochloride suppliers may include Lurasidone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Lurasidone Hydrochloride 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 Lurasidone Hydrochloride Drug Master File in Korea (Lurasidone Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Lurasidone Hydrochloride. The MFDS reviews the Lurasidone Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Lurasidone Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Lurasidone Hydrochloride 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 Lurasidone Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Lurasidone Hydrochloride suppliers with KDMF on PharmaCompass.
We have 2 companies offering Lurasidone Hydrochloride
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