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PharmaCompass offers a list of Magnesium Aspartate 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 Magnesium Aspartate manufacturer or Magnesium Aspartate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Magnesium Aspartate manufacturer or Magnesium Aspartate supplier.
PharmaCompass also assists you with knowing the Magnesium Aspartate API Price utilized in the formulation of products. Magnesium Aspartate API Price is not always fixed or binding as the Magnesium Aspartate Price is obtained through a variety of data sources. The Magnesium Aspartate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Magnesium Aspartate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Magnesium Aspartate, including repackagers and relabelers. The FDA regulates Magnesium Aspartate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Magnesium Aspartate 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 Magnesium Aspartate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Magnesium Aspartate supplier is an individual or a company that provides Magnesium Aspartate active pharmaceutical ingredient (API) or Magnesium Aspartate finished formulations upon request. The Magnesium Aspartate suppliers may include Magnesium Aspartate API manufacturers, exporters, distributors and traders.
click here to find a list of Magnesium Aspartate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Magnesium Aspartate Drug Master File in Japan (Magnesium Aspartate JDMF) empowers Magnesium Aspartate 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 Magnesium Aspartate JDMF during the approval evaluation for pharmaceutical products. At the time of Magnesium Aspartate 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 Magnesium Aspartate suppliers with JDMF on PharmaCompass.
Magnesium Aspartate 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 Magnesium Aspartate 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 Magnesium Aspartate GMP manufacturer or Magnesium Aspartate GMP API supplier for your needs.
A Magnesium Aspartate CoA (Certificate of Analysis) is a formal document that attests to Magnesium Aspartate's compliance with Magnesium Aspartate specifications and serves as a tool for batch-level quality control.
Magnesium Aspartate CoA mostly includes findings from lab analyses of a specific batch. For each Magnesium Aspartate 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.
Magnesium Aspartate may be tested according to a variety of international standards, such as European Pharmacopoeia (Magnesium Aspartate EP), Magnesium Aspartate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Magnesium Aspartate USP).