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ABOUT THIS PAGE
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PharmaCompass offers a list of Cefodizime Sodium 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 Cefodizime Sodium manufacturer or Cefodizime Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cefodizime Sodium manufacturer or Cefodizime Sodium supplier.
PharmaCompass also assists you with knowing the Cefodizime Sodium API Price utilized in the formulation of products. Cefodizime Sodium API Price is not always fixed or binding as the Cefodizime Sodium Price is obtained through a variety of data sources. The Cefodizime Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Modivid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Modivid, including repackagers and relabelers. The FDA regulates Modivid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Modivid API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Modivid supplier is an individual or a company that provides Modivid active pharmaceutical ingredient (API) or Modivid finished formulations upon request. The Modivid suppliers may include Modivid API manufacturers, exporters, distributors and traders.
click here to find a list of Modivid 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 Modivid Drug Master File in Korea (Modivid KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Modivid. The MFDS reviews the Modivid KDMF as part of the drug registration process and uses the information provided in the Modivid KDMF to evaluate the safety and efficacy of the drug.
After submitting a Modivid 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 Modivid API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Modivid suppliers with KDMF on PharmaCompass.
Modivid 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 Modivid 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 Modivid GMP manufacturer or Modivid GMP API supplier for your needs.
A Modivid CoA (Certificate of Analysis) is a formal document that attests to Modivid's compliance with Modivid specifications and serves as a tool for batch-level quality control.
Modivid CoA mostly includes findings from lab analyses of a specific batch. For each Modivid 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.
Modivid may be tested according to a variety of international standards, such as European Pharmacopoeia (Modivid EP), Modivid JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Modivid USP).
