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