Synopsis
0
USDMF
0
CEP/COS
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
EDQM
0
USP
0
JP
0
Others
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
API Reference Price
API/FDF Prices: Book a Demo to explore the features and consider upgrading later
API Imports and Exports
Market Place
ABOUT THIS PAGE
86
PharmaCompass offers a list of Sulbutiamine 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 Sulbutiamine manufacturer or Sulbutiamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sulbutiamine manufacturer or Sulbutiamine supplier.
PharmaCompass also assists you with knowing the Sulbutiamine API Price utilized in the formulation of products. Sulbutiamine API Price is not always fixed or binding as the Sulbutiamine Price is obtained through a variety of data sources. The Sulbutiamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Arcalion manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Arcalion, including repackagers and relabelers. The FDA regulates Arcalion manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Arcalion API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Arcalion supplier is an individual or a company that provides Arcalion active pharmaceutical ingredient (API) or Arcalion finished formulations upon request. The Arcalion suppliers may include Arcalion API manufacturers, exporters, distributors and traders.
click here to find a list of Arcalion 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 Arcalion Drug Master File in Japan (Arcalion JDMF) empowers Arcalion 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 Arcalion JDMF during the approval evaluation for pharmaceutical products. At the time of Arcalion 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 Arcalion suppliers with JDMF on PharmaCompass.
Arcalion 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 Arcalion 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 Arcalion GMP manufacturer or Arcalion GMP API supplier for your needs.
A Arcalion CoA (Certificate of Analysis) is a formal document that attests to Arcalion's compliance with Arcalion specifications and serves as a tool for batch-level quality control.
Arcalion CoA mostly includes findings from lab analyses of a specific batch. For each Arcalion 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.
Arcalion may be tested according to a variety of international standards, such as European Pharmacopoeia (Arcalion EP), Arcalion JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Arcalion USP).
