API Suppliers
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PharmaCompass offers a list of Vitamin E 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 Vitamin E manufacturer or Vitamin E supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Vitamin E manufacturer or Vitamin E supplier.
PharmaCompass also assists you with knowing the Vitamin E API Price utilized in the formulation of products. Vitamin E API Price is not always fixed or binding as the Vitamin E Price is obtained through a variety of data sources. The Vitamin E Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vitamin E Nicotinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vitamin E Nicotinate, including repackagers and relabelers. The FDA regulates Vitamin E Nicotinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vitamin E Nicotinate 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 Vitamin E Nicotinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vitamin E Nicotinate supplier is an individual or a company that provides Vitamin E Nicotinate active pharmaceutical ingredient (API) or Vitamin E Nicotinate finished formulations upon request. The Vitamin E Nicotinate suppliers may include Vitamin E Nicotinate API manufacturers, exporters, distributors and traders.
click here to find a list of Vitamin E Nicotinate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vitamin E Nicotinate DMF (Drug Master File) is a document detailing the whole manufacturing process of Vitamin E Nicotinate active pharmaceutical ingredient (API) in detail. Different forms of Vitamin E Nicotinate DMFs exist exist since differing nations have different regulations, such as Vitamin E Nicotinate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vitamin E Nicotinate DMF submitted to regulatory agencies in the US is known as a USDMF. Vitamin E Nicotinate USDMF includes data on Vitamin E Nicotinate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vitamin E Nicotinate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Vitamin E Nicotinate 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 Vitamin E Nicotinate Drug Master File in Japan (Vitamin E Nicotinate JDMF) empowers Vitamin E Nicotinate 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 Vitamin E Nicotinate JDMF during the approval evaluation for pharmaceutical products. At the time of Vitamin E Nicotinate 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 Vitamin E Nicotinate suppliers with JDMF on PharmaCompass.
A Vitamin E Nicotinate CEP of the European Pharmacopoeia monograph is often referred to as a Vitamin E Nicotinate Certificate of Suitability (COS). The purpose of a Vitamin E Nicotinate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Vitamin E Nicotinate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Vitamin E Nicotinate to their clients by showing that a Vitamin E Nicotinate CEP has been issued for it. The manufacturer submits a Vitamin E Nicotinate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Vitamin E Nicotinate CEP holder for the record. Additionally, the data presented in the Vitamin E Nicotinate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Vitamin E Nicotinate DMF.
A Vitamin E Nicotinate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Vitamin E Nicotinate 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 Vitamin E Nicotinate suppliers with CEP (COS) on PharmaCompass.
Vitamin E Nicotinate 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 Vitamin E Nicotinate 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 Vitamin E Nicotinate GMP manufacturer or Vitamin E Nicotinate GMP API supplier for your needs.
A Vitamin E Nicotinate CoA (Certificate of Analysis) is a formal document that attests to Vitamin E Nicotinate's compliance with Vitamin E Nicotinate specifications and serves as a tool for batch-level quality control.
Vitamin E Nicotinate CoA mostly includes findings from lab analyses of a specific batch. For each Vitamin E Nicotinate 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.
Vitamin E Nicotinate may be tested according to a variety of international standards, such as European Pharmacopoeia (Vitamin E Nicotinate EP), Vitamin E Nicotinate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Vitamin E Nicotinate USP).