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