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