X
API Suppliers
0
US DMFs Filed
0
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
0
0
0
USA (Orange Book)
0
Europe
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
0
U.S. Medicaid
0
Annual Reports
0
48
PharmaCompass offers a list of Edurant / Truvada 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 Edurant / Truvada manufacturer or Edurant / Truvada supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Edurant / Truvada manufacturer or Edurant / Truvada supplier.
PharmaCompass also assists you with knowing the Edurant / Truvada API Price utilized in the formulation of products. Edurant / Truvada API Price is not always fixed or binding as the Edurant / Truvada Price is obtained through a variety of data sources. The Edurant / Truvada Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Edurant / Truvada manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Edurant / Truvada, including repackagers and relabelers. The FDA regulates Edurant / Truvada manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Edurant / Truvada 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 Edurant / Truvada supplier is an individual or a company that provides Edurant / Truvada active pharmaceutical ingredient (API) or Edurant / Truvada finished formulations upon request. The Edurant / Truvada suppliers may include Edurant / Truvada API manufacturers, exporters, distributors and traders.
Edurant / Truvada 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 Edurant / Truvada 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 Edurant / Truvada GMP manufacturer or Edurant / Truvada GMP API supplier for your needs.
A Edurant / Truvada CoA (Certificate of Analysis) is a formal document that attests to Edurant / Truvada's compliance with Edurant / Truvada specifications and serves as a tool for batch-level quality control.
Edurant / Truvada CoA mostly includes findings from lab analyses of a specific batch. For each Edurant / Truvada 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.
Edurant / Truvada may be tested according to a variety of international standards, such as European Pharmacopoeia (Edurant / Truvada EP), Edurant / Truvada JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Edurant / Truvada USP).
Market Place
