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PharmaCompass offers a list of Zoledronic Acid 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 Zoledronic Acid manufacturer or Zoledronic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zoledronic Acid manufacturer or Zoledronic Acid supplier.
PharmaCompass also assists you with knowing the Zoledronic Acid API Price utilized in the formulation of products. Zoledronic Acid API Price is not always fixed or binding as the Zoledronic Acid Price is obtained through a variety of data sources. The Zoledronic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zoledronic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zoledronic Acid, including repackagers and relabelers. The FDA regulates Zoledronic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zoledronic Acid 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 Zoledronic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zoledronic Acid supplier is an individual or a company that provides Zoledronic Acid active pharmaceutical ingredient (API) or Zoledronic Acid finished formulations upon request. The Zoledronic Acid suppliers may include Zoledronic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Zoledronic Acid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zoledronic Acid DMF (Drug Master File) is a document detailing the whole manufacturing process of Zoledronic Acid active pharmaceutical ingredient (API) in detail. Different forms of Zoledronic Acid DMFs exist exist since differing nations have different regulations, such as Zoledronic Acid USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Zoledronic Acid DMF submitted to regulatory agencies in the US is known as a USDMF. Zoledronic Acid USDMF includes data on Zoledronic Acid's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Zoledronic Acid USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Zoledronic Acid 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 Zoledronic Acid Drug Master File in Japan (Zoledronic Acid JDMF) empowers Zoledronic Acid 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 Zoledronic Acid JDMF during the approval evaluation for pharmaceutical products. At the time of Zoledronic Acid 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 Zoledronic Acid suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Zoledronic Acid Drug Master File in Korea (Zoledronic Acid KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Zoledronic Acid. The MFDS reviews the Zoledronic Acid KDMF as part of the drug registration process and uses the information provided in the Zoledronic Acid KDMF to evaluate the safety and efficacy of the drug.
After submitting a Zoledronic Acid KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Zoledronic Acid API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Zoledronic Acid suppliers with KDMF on PharmaCompass.
A Zoledronic Acid CEP of the European Pharmacopoeia monograph is often referred to as a Zoledronic Acid Certificate of Suitability (COS). The purpose of a Zoledronic Acid CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Zoledronic Acid EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Zoledronic Acid to their clients by showing that a Zoledronic Acid CEP has been issued for it. The manufacturer submits a Zoledronic Acid CEP (COS) as part of the market authorization procedure, and it takes on the role of a Zoledronic Acid CEP holder for the record. Additionally, the data presented in the Zoledronic Acid CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Zoledronic Acid DMF.
A Zoledronic Acid CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Zoledronic Acid 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 Zoledronic Acid suppliers with CEP (COS) on PharmaCompass.
A Zoledronic Acid written confirmation (Zoledronic Acid WC) is an official document issued by a regulatory agency to a Zoledronic Acid manufacturer, verifying that the manufacturing facility of a Zoledronic Acid active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Zoledronic Acid APIs or Zoledronic Acid finished pharmaceutical products to another nation, regulatory agencies frequently require a Zoledronic Acid WC (written confirmation) as part of the regulatory process.
click here to find a list of Zoledronic Acid 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 Zoledronic Acid as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Zoledronic Acid 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 Zoledronic Acid 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 Zoledronic Acid and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zoledronic Acid NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Zoledronic Acid suppliers with NDC on PharmaCompass.
Zoledronic Acid 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 Zoledronic Acid 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 Zoledronic Acid GMP manufacturer or Zoledronic Acid GMP API supplier for your needs.
A Zoledronic Acid CoA (Certificate of Analysis) is a formal document that attests to Zoledronic Acid's compliance with Zoledronic Acid specifications and serves as a tool for batch-level quality control.
Zoledronic Acid CoA mostly includes findings from lab analyses of a specific batch. For each Zoledronic Acid 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.
Zoledronic Acid may be tested according to a variety of international standards, such as European Pharmacopoeia (Zoledronic Acid EP), Zoledronic Acid JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Zoledronic Acid USP).
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