API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
USA (Orange Book)
0
Europe
Canada
0
Australia
South Africa
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
0
11
PharmaCompass offers a list of Atazanavir 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 Atazanavir manufacturer or Atazanavir supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Atazanavir manufacturer or Atazanavir supplier.
PharmaCompass also assists you with knowing the Atazanavir API Price utilized in the formulation of products. Atazanavir API Price is not always fixed or binding as the Atazanavir Price is obtained through a variety of data sources. The Atazanavir Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Atazanavir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atazanavir, including repackagers and relabelers. The FDA regulates Atazanavir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atazanavir 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 Atazanavir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Atazanavir supplier is an individual or a company that provides Atazanavir active pharmaceutical ingredient (API) or Atazanavir finished formulations upon request. The Atazanavir suppliers may include Atazanavir API manufacturers, exporters, distributors and traders.
click here to find a list of Atazanavir suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Atazanavir DMF (Drug Master File) is a document detailing the whole manufacturing process of Atazanavir active pharmaceutical ingredient (API) in detail. Different forms of Atazanavir DMFs exist exist since differing nations have different regulations, such as Atazanavir USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Atazanavir DMF submitted to regulatory agencies in the US is known as a USDMF. Atazanavir USDMF includes data on Atazanavir's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Atazanavir USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Atazanavir suppliers with USDMF on PharmaCompass.
Atazanavir 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 Atazanavir 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 Atazanavir GMP manufacturer or Atazanavir GMP API supplier for your needs.
A Atazanavir CoA (Certificate of Analysis) is a formal document that attests to Atazanavir's compliance with Atazanavir specifications and serves as a tool for batch-level quality control.
Atazanavir CoA mostly includes findings from lab analyses of a specific batch. For each Atazanavir 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.
Atazanavir may be tested according to a variety of international standards, such as European Pharmacopoeia (Atazanavir EP), Atazanavir JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Atazanavir USP).