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ABOUT THIS PAGE
A Lanthanum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lanthanum, including repackagers and relabelers. The FDA regulates Lanthanum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lanthanum 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 Lanthanum supplier is an individual or a company that provides Lanthanum active pharmaceutical ingredient (API) or Lanthanum finished formulations upon request. The Lanthanum suppliers may include Lanthanum API manufacturers, exporters, distributors and traders.
Lanthanum 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 Lanthanum 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 Lanthanum GMP manufacturer or Lanthanum GMP API supplier for your needs.
A Lanthanum CoA (Certificate of Analysis) is a formal document that attests to Lanthanum's compliance with Lanthanum specifications and serves as a tool for batch-level quality control.
Lanthanum CoA mostly includes findings from lab analyses of a specific batch. For each Lanthanum 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.
Lanthanum may be tested according to a variety of international standards, such as European Pharmacopoeia (Lanthanum EP), Lanthanum JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lanthanum USP).
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