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SPI Pharma
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ABOUT THIS PAGE
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PharmaCompass offers a list of Granisetron Hydrochloride 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 Granisetron Hydrochloride manufacturer or Granisetron Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Granisetron Hydrochloride manufacturer or Granisetron Hydrochloride supplier.
PharmaCompass also assists you with knowing the Granisetron Hydrochloride API Price utilized in the formulation of products. Granisetron Hydrochloride API Price is not always fixed or binding as the Granisetron Hydrochloride Price is obtained through a variety of data sources. The Granisetron Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A AC-478 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AC-478, including repackagers and relabelers. The FDA regulates AC-478 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AC-478 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 AC-478 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AC-478 supplier is an individual or a company that provides AC-478 active pharmaceutical ingredient (API) or AC-478 finished formulations upon request. The AC-478 suppliers may include AC-478 API manufacturers, exporters, distributors and traders.
click here to find a list of AC-478 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A AC-478 DMF (Drug Master File) is a document detailing the whole manufacturing process of AC-478 active pharmaceutical ingredient (API) in detail. Different forms of AC-478 DMFs exist exist since differing nations have different regulations, such as AC-478 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A AC-478 DMF submitted to regulatory agencies in the US is known as a USDMF. AC-478 USDMF includes data on AC-478's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The AC-478 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of AC-478 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 AC-478 Drug Master File in Japan (AC-478 JDMF) empowers AC-478 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 AC-478 JDMF during the approval evaluation for pharmaceutical products. At the time of AC-478 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 AC-478 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 AC-478 Drug Master File in Korea (AC-478 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of AC-478. The MFDS reviews the AC-478 KDMF as part of the drug registration process and uses the information provided in the AC-478 KDMF to evaluate the safety and efficacy of the drug.
After submitting a AC-478 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 AC-478 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of AC-478 suppliers with KDMF on PharmaCompass.
A AC-478 CEP of the European Pharmacopoeia monograph is often referred to as a AC-478 Certificate of Suitability (COS). The purpose of a AC-478 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of AC-478 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of AC-478 to their clients by showing that a AC-478 CEP has been issued for it. The manufacturer submits a AC-478 CEP (COS) as part of the market authorization procedure, and it takes on the role of a AC-478 CEP holder for the record. Additionally, the data presented in the AC-478 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the AC-478 DMF.
A AC-478 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. AC-478 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 AC-478 suppliers with CEP (COS) on PharmaCompass.
A AC-478 written confirmation (AC-478 WC) is an official document issued by a regulatory agency to a AC-478 manufacturer, verifying that the manufacturing facility of a AC-478 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting AC-478 APIs or AC-478 finished pharmaceutical products to another nation, regulatory agencies frequently require a AC-478 WC (written confirmation) as part of the regulatory process.
click here to find a list of AC-478 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 AC-478 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for AC-478 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 AC-478 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 AC-478 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a AC-478 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of AC-478 suppliers with NDC on PharmaCompass.
AC-478 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 AC-478 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 AC-478 GMP manufacturer or AC-478 GMP API supplier for your needs.
A AC-478 CoA (Certificate of Analysis) is a formal document that attests to AC-478's compliance with AC-478 specifications and serves as a tool for batch-level quality control.
AC-478 CoA mostly includes findings from lab analyses of a specific batch. For each AC-478 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.
AC-478 may be tested according to a variety of international standards, such as European Pharmacopoeia (AC-478 EP), AC-478 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (AC-478 USP).
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
