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ABOUT THIS PAGE
A Podophyllum Resin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Podophyllum Resin, including repackagers and relabelers. The FDA regulates Podophyllum Resin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Podophyllum Resin 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 Podophyllum Resin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Podophyllum Resin supplier is an individual or a company that provides Podophyllum Resin active pharmaceutical ingredient (API) or Podophyllum Resin finished formulations upon request. The Podophyllum Resin suppliers may include Podophyllum Resin API manufacturers, exporters, distributors and traders.
click here to find a list of Podophyllum Resin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Podophyllum Resin written confirmation (Podophyllum Resin WC) is an official document issued by a regulatory agency to a Podophyllum Resin manufacturer, verifying that the manufacturing facility of a Podophyllum Resin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Podophyllum Resin APIs or Podophyllum Resin finished pharmaceutical products to another nation, regulatory agencies frequently require a Podophyllum Resin WC (written confirmation) as part of the regulatory process.
click here to find a list of Podophyllum Resin suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Podophyllum Resin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Podophyllum Resin API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Podophyllum Resin as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Podophyllum Resin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Podophyllum Resin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Podophyllum Resin suppliers with NDC on PharmaCompass.
Podophyllum Resin 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 Podophyllum Resin 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 Podophyllum Resin GMP manufacturer or Podophyllum Resin GMP API supplier for your needs.
A Podophyllum Resin CoA (Certificate of Analysis) is a formal document that attests to Podophyllum Resin's compliance with Podophyllum Resin specifications and serves as a tool for batch-level quality control.
Podophyllum Resin CoA mostly includes findings from lab analyses of a specific batch. For each Podophyllum Resin 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.
Podophyllum Resin may be tested according to a variety of international standards, such as European Pharmacopoeia (Podophyllum Resin EP), Podophyllum Resin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Podophyllum Resin USP).
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