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