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ABOUT THIS PAGE
A Glycerylphosphorylcholine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glycerylphosphorylcholine, including repackagers and relabelers. The FDA regulates Glycerylphosphorylcholine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glycerylphosphorylcholine 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 Glycerylphosphorylcholine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glycerylphosphorylcholine supplier is an individual or a company that provides Glycerylphosphorylcholine active pharmaceutical ingredient (API) or Glycerylphosphorylcholine finished formulations upon request. The Glycerylphosphorylcholine suppliers may include Glycerylphosphorylcholine API manufacturers, exporters, distributors and traders.
click here to find a list of Glycerylphosphorylcholine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Glycerylphosphorylcholine DMF (Drug Master File) is a document detailing the whole manufacturing process of Glycerylphosphorylcholine active pharmaceutical ingredient (API) in detail. Different forms of Glycerylphosphorylcholine DMFs exist exist since differing nations have different regulations, such as Glycerylphosphorylcholine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Glycerylphosphorylcholine DMF submitted to regulatory agencies in the US is known as a USDMF. Glycerylphosphorylcholine USDMF includes data on Glycerylphosphorylcholine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Glycerylphosphorylcholine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Glycerylphosphorylcholine 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 Glycerylphosphorylcholine Drug Master File in Korea (Glycerylphosphorylcholine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Glycerylphosphorylcholine. The MFDS reviews the Glycerylphosphorylcholine KDMF as part of the drug registration process and uses the information provided in the Glycerylphosphorylcholine KDMF to evaluate the safety and efficacy of the drug.
After submitting a Glycerylphosphorylcholine 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 Glycerylphosphorylcholine API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Glycerylphosphorylcholine 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 Glycerylphosphorylcholine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Glycerylphosphorylcholine 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 Glycerylphosphorylcholine 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 Glycerylphosphorylcholine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Glycerylphosphorylcholine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Glycerylphosphorylcholine suppliers with NDC on PharmaCompass.
Glycerylphosphorylcholine 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 Glycerylphosphorylcholine 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 Glycerylphosphorylcholine GMP manufacturer or Glycerylphosphorylcholine GMP API supplier for your needs.
A Glycerylphosphorylcholine CoA (Certificate of Analysis) is a formal document that attests to Glycerylphosphorylcholine's compliance with Glycerylphosphorylcholine specifications and serves as a tool for batch-level quality control.
Glycerylphosphorylcholine CoA mostly includes findings from lab analyses of a specific batch. For each Glycerylphosphorylcholine 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.
Glycerylphosphorylcholine may be tested according to a variety of international standards, such as European Pharmacopoeia (Glycerylphosphorylcholine EP), Glycerylphosphorylcholine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Glycerylphosphorylcholine USP).
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