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PharmaCompass offers a list of Zaltoprofen 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 Zaltoprofen manufacturer or Zaltoprofen supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zaltoprofen manufacturer or Zaltoprofen supplier.
PharmaCompass also assists you with knowing the Zaltoprofen API Price utilized in the formulation of products. Zaltoprofen API Price is not always fixed or binding as the Zaltoprofen Price is obtained through a variety of data sources. The Zaltoprofen Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zaltoprofene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zaltoprofene, including repackagers and relabelers. The FDA regulates Zaltoprofene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zaltoprofene 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 Zaltoprofene manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zaltoprofene supplier is an individual or a company that provides Zaltoprofene active pharmaceutical ingredient (API) or Zaltoprofene finished formulations upon request. The Zaltoprofene suppliers may include Zaltoprofene API manufacturers, exporters, distributors and traders.
click here to find a list of Zaltoprofene suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information 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 Zaltoprofene Drug Master File in Japan (Zaltoprofene JDMF) empowers Zaltoprofene 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 Zaltoprofene JDMF during the approval evaluation for pharmaceutical products. At the time of Zaltoprofene 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 Zaltoprofene 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 Zaltoprofene Drug Master File in Korea (Zaltoprofene KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Zaltoprofene. The MFDS reviews the Zaltoprofene KDMF as part of the drug registration process and uses the information provided in the Zaltoprofene KDMF to evaluate the safety and efficacy of the drug.
After submitting a Zaltoprofene 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 Zaltoprofene API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Zaltoprofene suppliers with KDMF on PharmaCompass.
A Zaltoprofene written confirmation (Zaltoprofene WC) is an official document issued by a regulatory agency to a Zaltoprofene manufacturer, verifying that the manufacturing facility of a Zaltoprofene active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Zaltoprofene APIs or Zaltoprofene finished pharmaceutical products to another nation, regulatory agencies frequently require a Zaltoprofene WC (written confirmation) as part of the regulatory process.
click here to find a list of Zaltoprofene suppliers with Written Confirmation (WC) on PharmaCompass.
Zaltoprofene 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 Zaltoprofene 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 Zaltoprofene GMP manufacturer or Zaltoprofene GMP API supplier for your needs.
A Zaltoprofene CoA (Certificate of Analysis) is a formal document that attests to Zaltoprofene's compliance with Zaltoprofene specifications and serves as a tool for batch-level quality control.
Zaltoprofene CoA mostly includes findings from lab analyses of a specific batch. For each Zaltoprofene 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.
Zaltoprofene may be tested according to a variety of international standards, such as European Pharmacopoeia (Zaltoprofene EP), Zaltoprofene JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Zaltoprofene USP).
