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PharmaCompass offers a list of Levosulpiride 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 Levosulpiride manufacturer or Levosulpiride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Levosulpiride manufacturer or Levosulpiride supplier.
PharmaCompass also assists you with knowing the Levosulpiride API Price utilized in the formulation of products. Levosulpiride API Price is not always fixed or binding as the Levosulpiride Price is obtained through a variety of data sources. The Levosulpiride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Levosulpiride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levosulpiride, including repackagers and relabelers. The FDA regulates Levosulpiride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levosulpiride 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 Levosulpiride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levosulpiride supplier is an individual or a company that provides Levosulpiride active pharmaceutical ingredient (API) or Levosulpiride finished formulations upon request. The Levosulpiride suppliers may include Levosulpiride API manufacturers, exporters, distributors and traders.
click here to find a list of Levosulpiride 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 Levosulpiride Drug Master File in Korea (Levosulpiride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Levosulpiride. The MFDS reviews the Levosulpiride KDMF as part of the drug registration process and uses the information provided in the Levosulpiride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Levosulpiride 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 Levosulpiride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Levosulpiride suppliers with KDMF on PharmaCompass.
A Levosulpiride written confirmation (Levosulpiride WC) is an official document issued by a regulatory agency to a Levosulpiride manufacturer, verifying that the manufacturing facility of a Levosulpiride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Levosulpiride APIs or Levosulpiride finished pharmaceutical products to another nation, regulatory agencies frequently require a Levosulpiride WC (written confirmation) as part of the regulatory process.
click here to find a list of Levosulpiride suppliers with Written Confirmation (WC) on PharmaCompass.
Levosulpiride Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Levosulpiride GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Levosulpiride GMP manufacturer or Levosulpiride GMP API supplier for your needs.
A Levosulpiride CoA (Certificate of Analysis) is a formal document that attests to Levosulpiride's compliance with Levosulpiride specifications and serves as a tool for batch-level quality control.
Levosulpiride CoA mostly includes findings from lab analyses of a specific batch. For each Levosulpiride CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Levosulpiride may be tested according to a variety of international standards, such as European Pharmacopoeia (Levosulpiride EP), Levosulpiride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Levosulpiride USP).
