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