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