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API SUPPLIERS
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USDMF
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SPI Pharma
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Arthrocine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Arthrocine, including repackagers and relabelers. The FDA regulates Arthrocine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Arthrocine 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 Arthrocine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Arthrocine supplier is an individual or a company that provides Arthrocine active pharmaceutical ingredient (API) or Arthrocine finished formulations upon request. The Arthrocine suppliers may include Arthrocine API manufacturers, exporters, distributors and traders.
click here to find a list of Arthrocine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Arthrocine DMF (Drug Master File) is a document detailing the whole manufacturing process of Arthrocine active pharmaceutical ingredient (API) in detail. Different forms of Arthrocine DMFs exist exist since differing nations have different regulations, such as Arthrocine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Arthrocine DMF submitted to regulatory agencies in the US is known as a USDMF. Arthrocine USDMF includes data on Arthrocine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Arthrocine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Arthrocine 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 Arthrocine Drug Master File in Japan (Arthrocine JDMF) empowers Arthrocine 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 Arthrocine JDMF during the approval evaluation for pharmaceutical products. At the time of Arthrocine 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 Arthrocine suppliers with JDMF on PharmaCompass.
A Arthrocine written confirmation (Arthrocine WC) is an official document issued by a regulatory agency to a Arthrocine manufacturer, verifying that the manufacturing facility of a Arthrocine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Arthrocine APIs or Arthrocine finished pharmaceutical products to another nation, regulatory agencies frequently require a Arthrocine WC (written confirmation) as part of the regulatory process.
click here to find a list of Arthrocine 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 Arthrocine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Arthrocine 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 Arthrocine 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 Arthrocine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Arthrocine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Arthrocine suppliers with NDC on PharmaCompass.
Arthrocine 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 Arthrocine 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 Arthrocine GMP manufacturer or Arthrocine GMP API supplier for your needs.
A Arthrocine CoA (Certificate of Analysis) is a formal document that attests to Arthrocine's compliance with Arthrocine specifications and serves as a tool for batch-level quality control.
Arthrocine CoA mostly includes findings from lab analyses of a specific batch. For each Arthrocine 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.
Arthrocine may be tested according to a variety of international standards, such as European Pharmacopoeia (Arthrocine EP), Arthrocine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Arthrocine USP).
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