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ABOUT THIS PAGE
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PharmaCompass offers a list of Glycerylphosphorylcholine 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 Glycerylphosphorylcholine manufacturer or Glycerylphosphorylcholine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glycerylphosphorylcholine manufacturer or Glycerylphosphorylcholine supplier.
PharmaCompass also assists you with knowing the Glycerylphosphorylcholine API Price utilized in the formulation of products. Glycerylphosphorylcholine API Price is not always fixed or binding as the Glycerylphosphorylcholine Price is obtained through a variety of data sources. The Glycerylphosphorylcholine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Alpha GPC manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alpha GPC, including repackagers and relabelers. The FDA regulates Alpha GPC manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alpha GPC 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 Alpha GPC manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Alpha GPC supplier is an individual or a company that provides Alpha GPC active pharmaceutical ingredient (API) or Alpha GPC finished formulations upon request. The Alpha GPC suppliers may include Alpha GPC API manufacturers, exporters, distributors and traders.
click here to find a list of Alpha GPC suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Alpha GPC DMF (Drug Master File) is a document detailing the whole manufacturing process of Alpha GPC active pharmaceutical ingredient (API) in detail. Different forms of Alpha GPC DMFs exist exist since differing nations have different regulations, such as Alpha GPC USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Alpha GPC DMF submitted to regulatory agencies in the US is known as a USDMF. Alpha GPC USDMF includes data on Alpha GPC's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Alpha GPC USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Alpha GPC suppliers with USDMF 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 Alpha GPC Drug Master File in Korea (Alpha GPC KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Alpha GPC. The MFDS reviews the Alpha GPC KDMF as part of the drug registration process and uses the information provided in the Alpha GPC KDMF to evaluate the safety and efficacy of the drug.
After submitting a Alpha GPC 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 Alpha GPC API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Alpha GPC suppliers with KDMF on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Alpha GPC as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Alpha GPC API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Alpha GPC as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Alpha GPC and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Alpha GPC NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Alpha GPC suppliers with NDC on PharmaCompass.
Alpha GPC 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 Alpha GPC 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 Alpha GPC GMP manufacturer or Alpha GPC GMP API supplier for your needs.
A Alpha GPC CoA (Certificate of Analysis) is a formal document that attests to Alpha GPC's compliance with Alpha GPC specifications and serves as a tool for batch-level quality control.
Alpha GPC CoA mostly includes findings from lab analyses of a specific batch. For each Alpha GPC 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.
Alpha GPC may be tested according to a variety of international standards, such as European Pharmacopoeia (Alpha GPC EP), Alpha GPC JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Alpha GPC USP).
