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API SUPPLIERS
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JDMF
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Tagoor's product development expertise, backed by our comprehensive understanding of the processes, helps us offer high-quality APIs.
CAS Number : 5382-16-1
End Use API : propericiazine
About The Company : Tagoor Laboratories, established in 2018, is a part of the Tagoor Group. It specializes in providing APIs, advanced intermediates and key starting materials for...
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ABOUT THIS PAGE
A propericiazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of propericiazine, including repackagers and relabelers. The FDA regulates propericiazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. propericiazine 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 propericiazine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A propericiazine supplier is an individual or a company that provides propericiazine active pharmaceutical ingredient (API) or propericiazine finished formulations upon request. The propericiazine suppliers may include propericiazine API manufacturers, exporters, distributors and traders.
click here to find a list of propericiazine 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 propericiazine Drug Master File in Japan (propericiazine JDMF) empowers propericiazine 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 propericiazine JDMF during the approval evaluation for pharmaceutical products. At the time of propericiazine 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 propericiazine suppliers with JDMF on PharmaCompass.
propericiazine 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 propericiazine 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 propericiazine GMP manufacturer or propericiazine GMP API supplier for your needs.
A propericiazine CoA (Certificate of Analysis) is a formal document that attests to propericiazine's compliance with propericiazine specifications and serves as a tool for batch-level quality control.
propericiazine CoA mostly includes findings from lab analyses of a specific batch. For each propericiazine 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.
propericiazine may be tested according to a variety of international standards, such as European Pharmacopoeia (propericiazine EP), propericiazine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (propericiazine USP).
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