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API SUPPLIERS
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CEP/COS
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Bromperidol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bromperidol, including repackagers and relabelers. The FDA regulates Bromperidol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bromperidol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Bromperidol supplier is an individual or a company that provides Bromperidol active pharmaceutical ingredient (API) or Bromperidol finished formulations upon request. The Bromperidol suppliers may include Bromperidol API manufacturers, exporters, distributors and traders.
click here to find a list of Bromperidol 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 Bromperidol Drug Master File in Japan (Bromperidol JDMF) empowers Bromperidol 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 Bromperidol JDMF during the approval evaluation for pharmaceutical products. At the time of Bromperidol 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 Bromperidol suppliers with JDMF on PharmaCompass.
A Bromperidol CEP of the European Pharmacopoeia monograph is often referred to as a Bromperidol Certificate of Suitability (COS). The purpose of a Bromperidol CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Bromperidol EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Bromperidol to their clients by showing that a Bromperidol CEP has been issued for it. The manufacturer submits a Bromperidol CEP (COS) as part of the market authorization procedure, and it takes on the role of a Bromperidol CEP holder for the record. Additionally, the data presented in the Bromperidol CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Bromperidol DMF.
A Bromperidol CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Bromperidol 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 Bromperidol suppliers with CEP (COS) on PharmaCompass.
Bromperidol 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 Bromperidol 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 Bromperidol GMP manufacturer or Bromperidol GMP API supplier for your needs.
A Bromperidol CoA (Certificate of Analysis) is a formal document that attests to Bromperidol's compliance with Bromperidol specifications and serves as a tool for batch-level quality control.
Bromperidol CoA mostly includes findings from lab analyses of a specific batch. For each Bromperidol 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.
Bromperidol may be tested according to a variety of international standards, such as European Pharmacopoeia (Bromperidol EP), Bromperidol JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Bromperidol USP).
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