X
API Suppliers
US DMFs Filed
CEP/COS Certifications
JDMFs Filed
Other Certificates
Other Suppliers
0
USA (Orange Book)
0
Europe
0
Canada
Australia
0
South Africa
Uploaded Dossiers
0
U.S. Medicaid
0
Annual Reports
0
17
PharmaCompass offers a list of L-Glutamic Acid 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 L-Glutamic Acid manufacturer or L-Glutamic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred L-Glutamic Acid manufacturer or L-Glutamic Acid supplier.
PharmaCompass also assists you with knowing the L-Glutamic Acid API Price utilized in the formulation of products. L-Glutamic Acid API Price is not always fixed or binding as the L-Glutamic Acid Price is obtained through a variety of data sources. The L-Glutamic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Aluminum L Glutamate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aluminum L Glutamate, including repackagers and relabelers. The FDA regulates Aluminum L Glutamate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aluminum L Glutamate 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 Aluminum L Glutamate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Aluminum L Glutamate supplier is an individual or a company that provides Aluminum L Glutamate active pharmaceutical ingredient (API) or Aluminum L Glutamate finished formulations upon request. The Aluminum L Glutamate suppliers may include Aluminum L Glutamate API manufacturers, exporters, distributors and traders.
click here to find a list of Aluminum L Glutamate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Aluminum L Glutamate DMF (Drug Master File) is a document detailing the whole manufacturing process of Aluminum L Glutamate active pharmaceutical ingredient (API) in detail. Different forms of Aluminum L Glutamate DMFs exist exist since differing nations have different regulations, such as Aluminum L Glutamate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Aluminum L Glutamate DMF submitted to regulatory agencies in the US is known as a USDMF. Aluminum L Glutamate USDMF includes data on Aluminum L Glutamate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Aluminum L Glutamate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Aluminum L Glutamate suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Aluminum L Glutamate Drug Master File in Japan (Aluminum L Glutamate JDMF) empowers Aluminum L Glutamate API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Aluminum L Glutamate JDMF during the approval evaluation for pharmaceutical products. At the time of Aluminum L Glutamate JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Aluminum L Glutamate suppliers with JDMF on PharmaCompass.
A Aluminum L Glutamate CEP of the European Pharmacopoeia monograph is often referred to as a Aluminum L Glutamate Certificate of Suitability (COS). The purpose of a Aluminum L Glutamate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Aluminum L Glutamate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Aluminum L Glutamate to their clients by showing that a Aluminum L Glutamate CEP has been issued for it. The manufacturer submits a Aluminum L Glutamate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Aluminum L Glutamate CEP holder for the record. Additionally, the data presented in the Aluminum L Glutamate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Aluminum L Glutamate DMF.
A Aluminum L Glutamate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Aluminum L Glutamate CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Aluminum L Glutamate suppliers with CEP (COS) on PharmaCompass.
A Aluminum L Glutamate written confirmation (Aluminum L Glutamate WC) is an official document issued by a regulatory agency to a Aluminum L Glutamate manufacturer, verifying that the manufacturing facility of a Aluminum L Glutamate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Aluminum L Glutamate APIs or Aluminum L Glutamate finished pharmaceutical products to another nation, regulatory agencies frequently require a Aluminum L Glutamate WC (written confirmation) as part of the regulatory process.
click here to find a list of Aluminum L Glutamate suppliers with Written Confirmation (WC) 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 Aluminum L Glutamate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Aluminum L Glutamate 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 Aluminum L Glutamate 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 Aluminum L Glutamate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Aluminum L Glutamate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Aluminum L Glutamate suppliers with NDC on PharmaCompass.
Aluminum L Glutamate 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 Aluminum L Glutamate 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 Aluminum L Glutamate GMP manufacturer or Aluminum L Glutamate GMP API supplier for your needs.
A Aluminum L Glutamate CoA (Certificate of Analysis) is a formal document that attests to Aluminum L Glutamate's compliance with Aluminum L Glutamate specifications and serves as a tool for batch-level quality control.
Aluminum L Glutamate CoA mostly includes findings from lab analyses of a specific batch. For each Aluminum L Glutamate 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.
Aluminum L Glutamate may be tested according to a variety of international standards, such as European Pharmacopoeia (Aluminum L Glutamate EP), Aluminum L Glutamate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Aluminum L Glutamate USP).
Market Place
