X
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
0
South Africa
Uploaded Dossiers
0
U.S. Medicaid
Annual Reports
0
0
15
PharmaCompass offers a list of Rosiglitazone 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 Rosiglitazone manufacturer or Rosiglitazone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rosiglitazone manufacturer or Rosiglitazone supplier.
PharmaCompass also assists you with knowing the Rosiglitazone API Price utilized in the formulation of products. Rosiglitazone API Price is not always fixed or binding as the Rosiglitazone Price is obtained through a variety of data sources. The Rosiglitazone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rosiglitazone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rosiglitazone, including repackagers and relabelers. The FDA regulates Rosiglitazone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rosiglitazone 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 Rosiglitazone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rosiglitazone supplier is an individual or a company that provides Rosiglitazone active pharmaceutical ingredient (API) or Rosiglitazone finished formulations upon request. The Rosiglitazone suppliers may include Rosiglitazone API manufacturers, exporters, distributors and traders.
click here to find a list of Rosiglitazone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rosiglitazone DMF (Drug Master File) is a document detailing the whole manufacturing process of Rosiglitazone active pharmaceutical ingredient (API) in detail. Different forms of Rosiglitazone DMFs exist exist since differing nations have different regulations, such as Rosiglitazone USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Rosiglitazone DMF submitted to regulatory agencies in the US is known as a USDMF. Rosiglitazone USDMF includes data on Rosiglitazone's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Rosiglitazone USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Rosiglitazone suppliers with USDMF on PharmaCompass.
Rosiglitazone 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 Rosiglitazone 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 Rosiglitazone GMP manufacturer or Rosiglitazone GMP API supplier for your needs.
A Rosiglitazone CoA (Certificate of Analysis) is a formal document that attests to Rosiglitazone's compliance with Rosiglitazone specifications and serves as a tool for batch-level quality control.
Rosiglitazone CoA mostly includes findings from lab analyses of a specific batch. For each Rosiglitazone 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.
Rosiglitazone may be tested according to a variety of international standards, such as European Pharmacopoeia (Rosiglitazone EP), Rosiglitazone JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Rosiglitazone USP).
Market Place
