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