API Suppliers
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EDQM
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PharmaCompass offers a list of lime 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 lime manufacturer or lime supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred lime manufacturer or lime supplier.
PharmaCompass also assists you with knowing the lime API Price utilized in the formulation of products. lime API Price is not always fixed or binding as the lime Price is obtained through a variety of data sources. The lime Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A lime manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of lime, including repackagers and relabelers. The FDA regulates lime manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. lime 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 lime supplier is an individual or a company that provides lime active pharmaceutical ingredient (API) or lime finished formulations upon request. The lime suppliers may include lime API manufacturers, exporters, distributors and traders.
click here to find a list of lime suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A lime DMF (Drug Master File) is a document detailing the whole manufacturing process of lime active pharmaceutical ingredient (API) in detail. Different forms of lime DMFs exist exist since differing nations have different regulations, such as lime USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A lime DMF submitted to regulatory agencies in the US is known as a USDMF. lime USDMF includes data on lime's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The lime USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of lime suppliers with USDMF on PharmaCompass.
lime 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 lime 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 lime GMP manufacturer or lime GMP API supplier for your needs.
A lime CoA (Certificate of Analysis) is a formal document that attests to lime's compliance with lime specifications and serves as a tool for batch-level quality control.
lime CoA mostly includes findings from lab analyses of a specific batch. For each lime 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.
lime may be tested according to a variety of international standards, such as European Pharmacopoeia (lime EP), lime JP (Japanese Pharmacopeia) and the US Pharmacopoeia (lime USP).