X
API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
0
USA (Orange Book)
0
Europe
0
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
0
45
PharmaCompass offers a list of Maltose 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 Maltose manufacturer or Maltose supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Maltose manufacturer or Maltose supplier.
PharmaCompass also assists you with knowing the Maltose API Price utilized in the formulation of products. Maltose API Price is not always fixed or binding as the Maltose Price is obtained through a variety of data sources. The Maltose Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Maltose manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Maltose, including repackagers and relabelers. The FDA regulates Maltose manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Maltose 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 Maltose manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Maltose supplier is an individual or a company that provides Maltose active pharmaceutical ingredient (API) or Maltose finished formulations upon request. The Maltose suppliers may include Maltose API manufacturers, exporters, distributors and traders.
click here to find a list of Maltose suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Maltose DMF (Drug Master File) is a document detailing the whole manufacturing process of Maltose active pharmaceutical ingredient (API) in detail. Different forms of Maltose DMFs exist exist since differing nations have different regulations, such as Maltose USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Maltose DMF submitted to regulatory agencies in the US is known as a USDMF. Maltose USDMF includes data on Maltose's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Maltose USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Maltose suppliers with USDMF on PharmaCompass.
Maltose 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 Maltose 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 Maltose GMP manufacturer or Maltose GMP API supplier for your needs.
A Maltose CoA (Certificate of Analysis) is a formal document that attests to Maltose's compliance with Maltose specifications and serves as a tool for batch-level quality control.
Maltose CoA mostly includes findings from lab analyses of a specific batch. For each Maltose 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.
Maltose may be tested according to a variety of international standards, such as European Pharmacopoeia (Maltose EP), Maltose JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Maltose USP).
Market Place
