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PharmaCompass offers a list of Vitamin D3 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 Vitamin D3 manufacturer or Vitamin D3 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin D3 manufacturer or Vitamin D3 supplier.
PharmaCompass also assists you with knowing the Vitamin D3 API Price utilized in the formulation of products. Vitamin D3 API Price is not always fixed or binding as the Vitamin D3 Price is obtained through a variety of data sources. The Vitamin D3 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cholecalciferol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cholecalciferol, including repackagers and relabelers. The FDA regulates Cholecalciferol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cholecalciferol 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 Cholecalciferol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cholecalciferol supplier is an individual or a company that provides Cholecalciferol active pharmaceutical ingredient (API) or Cholecalciferol finished formulations upon request. The Cholecalciferol suppliers may include Cholecalciferol API manufacturers, exporters, distributors and traders.
click here to find a list of Cholecalciferol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cholecalciferol DMF (Drug Master File) is a document detailing the whole manufacturing process of Cholecalciferol active pharmaceutical ingredient (API) in detail. Different forms of Cholecalciferol DMFs exist exist since differing nations have different regulations, such as Cholecalciferol USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cholecalciferol DMF submitted to regulatory agencies in the US is known as a USDMF. Cholecalciferol USDMF includes data on Cholecalciferol's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cholecalciferol USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cholecalciferol suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Cholecalciferol Drug Master File in Japan (Cholecalciferol JDMF) empowers Cholecalciferol API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Cholecalciferol JDMF during the approval evaluation for pharmaceutical products. At the time of Cholecalciferol JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Cholecalciferol suppliers with JDMF on PharmaCompass.
A Cholecalciferol CEP of the European Pharmacopoeia monograph is often referred to as a Cholecalciferol Certificate of Suitability (COS). The purpose of a Cholecalciferol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cholecalciferol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cholecalciferol to their clients by showing that a Cholecalciferol CEP has been issued for it. The manufacturer submits a Cholecalciferol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cholecalciferol CEP holder for the record. Additionally, the data presented in the Cholecalciferol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cholecalciferol DMF.
A Cholecalciferol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cholecalciferol CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Cholecalciferol suppliers with CEP (COS) on PharmaCompass.
A Cholecalciferol written confirmation (Cholecalciferol WC) is an official document issued by a regulatory agency to a Cholecalciferol manufacturer, verifying that the manufacturing facility of a Cholecalciferol active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Cholecalciferol APIs or Cholecalciferol finished pharmaceutical products to another nation, regulatory agencies frequently require a Cholecalciferol WC (written confirmation) as part of the regulatory process.
click here to find a list of Cholecalciferol 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 Cholecalciferol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cholecalciferol 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 Cholecalciferol 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 Cholecalciferol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cholecalciferol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cholecalciferol suppliers with NDC on PharmaCompass.
Cholecalciferol 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 Cholecalciferol 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 Cholecalciferol GMP manufacturer or Cholecalciferol GMP API supplier for your needs.
A Cholecalciferol CoA (Certificate of Analysis) is a formal document that attests to Cholecalciferol's compliance with Cholecalciferol specifications and serves as a tool for batch-level quality control.
Cholecalciferol CoA mostly includes findings from lab analyses of a specific batch. For each Cholecalciferol 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.
Cholecalciferol may be tested according to a variety of international standards, such as European Pharmacopoeia (Cholecalciferol EP), Cholecalciferol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cholecalciferol USP).
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