X
API Suppliers
US DMFs Filed
0
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
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
85
PharmaCompass offers a list of Vadadustat 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 Vadadustat manufacturer or Vadadustat supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vadadustat manufacturer or Vadadustat supplier.
PharmaCompass also assists you with knowing the Vadadustat API Price utilized in the formulation of products. Vadadustat API Price is not always fixed or binding as the Vadadustat Price is obtained through a variety of data sources. The Vadadustat Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AKB-6548 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AKB-6548, including repackagers and relabelers. The FDA regulates AKB-6548 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AKB-6548 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 AKB-6548 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AKB-6548 supplier is an individual or a company that provides AKB-6548 active pharmaceutical ingredient (API) or AKB-6548 finished formulations upon request. The AKB-6548 suppliers may include AKB-6548 API manufacturers, exporters, distributors and traders.
click here to find a list of AKB-6548 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a AKB-6548 Drug Master File in Korea (AKB-6548 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of AKB-6548. The MFDS reviews the AKB-6548 KDMF as part of the drug registration process and uses the information provided in the AKB-6548 KDMF to evaluate the safety and efficacy of the drug.
After submitting a AKB-6548 KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their AKB-6548 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of AKB-6548 suppliers with KDMF on PharmaCompass.
AKB-6548 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 AKB-6548 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 AKB-6548 GMP manufacturer or AKB-6548 GMP API supplier for your needs.
A AKB-6548 CoA (Certificate of Analysis) is a formal document that attests to AKB-6548's compliance with AKB-6548 specifications and serves as a tool for batch-level quality control.
AKB-6548 CoA mostly includes findings from lab analyses of a specific batch. For each AKB-6548 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.
AKB-6548 may be tested according to a variety of international standards, such as European Pharmacopoeia (AKB-6548 EP), AKB-6548 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AKB-6548 USP).
Market Place
