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
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
ABOUT THIS PAGE
24
PharmaCompass offers a list of P-N-Methylaminoazobenzene 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 P-N-Methylaminoazobenzene manufacturer or P-N-Methylaminoazobenzene supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred P-N-Methylaminoazobenzene manufacturer or P-N-Methylaminoazobenzene supplier.
PharmaCompass also assists you with knowing the P-N-Methylaminoazobenzene API Price utilized in the formulation of products. P-N-Methylaminoazobenzene API Price is not always fixed or binding as the P-N-Methylaminoazobenzene Price is obtained through a variety of data sources. The P-N-Methylaminoazobenzene Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MAB manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MAB, including repackagers and relabelers. The FDA regulates MAB manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MAB 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 MAB supplier is an individual or a company that provides MAB active pharmaceutical ingredient (API) or MAB finished formulations upon request. The MAB suppliers may include MAB API manufacturers, exporters, distributors and traders.
click here to find a list of MAB 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 MAB Drug Master File in Japan (MAB JDMF) empowers MAB 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 MAB JDMF during the approval evaluation for pharmaceutical products. At the time of MAB 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 MAB suppliers with JDMF on PharmaCompass.
MAB 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 MAB 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 MAB GMP manufacturer or MAB GMP API supplier for your needs.
A MAB CoA (Certificate of Analysis) is a formal document that attests to MAB's compliance with MAB specifications and serves as a tool for batch-level quality control.
MAB CoA mostly includes findings from lab analyses of a specific batch. For each MAB 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.
MAB may be tested according to a variety of international standards, such as European Pharmacopoeia (MAB EP), MAB JP (Japanese Pharmacopeia) and the US Pharmacopoeia (MAB USP).
