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
0
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
0
U.S. Medicaid
0
Annual Reports
0
0
43
PharmaCompass offers a list of Gefarnate 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 Gefarnate manufacturer or Gefarnate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Gefarnate manufacturer or Gefarnate supplier.
PharmaCompass also assists you with knowing the Gefarnate API Price utilized in the formulation of products. Gefarnate API Price is not always fixed or binding as the Gefarnate Price is obtained through a variety of data sources. The Gefarnate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gefarnate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gefarnate, including repackagers and relabelers. The FDA regulates Gefarnate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gefarnate 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 Gefarnate supplier is an individual or a company that provides Gefarnate active pharmaceutical ingredient (API) or Gefarnate finished formulations upon request. The Gefarnate suppliers may include Gefarnate API manufacturers, exporters, distributors and traders.
Gefarnate 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 Gefarnate 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 Gefarnate GMP manufacturer or Gefarnate GMP API supplier for your needs.
A Gefarnate CoA (Certificate of Analysis) is a formal document that attests to Gefarnate's compliance with Gefarnate specifications and serves as a tool for batch-level quality control.
Gefarnate CoA mostly includes findings from lab analyses of a specific batch. For each Gefarnate 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.
Gefarnate may be tested according to a variety of international standards, such as European Pharmacopoeia (Gefarnate EP), Gefarnate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Gefarnate USP).