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PharmaCompass offers a list of Diethylhexyl Phthalate 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 Diethylhexyl Phthalate manufacturer or Diethylhexyl Phthalate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diethylhexyl Phthalate manufacturer or Diethylhexyl Phthalate supplier.
PharmaCompass also assists you with knowing the Diethylhexyl Phthalate API Price utilized in the formulation of products. Diethylhexyl Phthalate API Price is not always fixed or binding as the Diethylhexyl Phthalate Price is obtained through a variety of data sources. The Diethylhexyl Phthalate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diethylhexyl Phthalate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diethylhexyl Phthalate, including repackagers and relabelers. The FDA regulates Diethylhexyl Phthalate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diethylhexyl Phthalate 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 Diethylhexyl Phthalate supplier is an individual or a company that provides Diethylhexyl Phthalate active pharmaceutical ingredient (API) or Diethylhexyl Phthalate finished formulations upon request. The Diethylhexyl Phthalate suppliers may include Diethylhexyl Phthalate API manufacturers, exporters, distributors and traders.
click here to find a list of Diethylhexyl Phthalate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Diethylhexyl Phthalate DMF (Drug Master File) is a document detailing the whole manufacturing process of Diethylhexyl Phthalate active pharmaceutical ingredient (API) in detail. Different forms of Diethylhexyl Phthalate DMFs exist exist since differing nations have different regulations, such as Diethylhexyl Phthalate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Diethylhexyl Phthalate DMF submitted to regulatory agencies in the US is known as a USDMF. Diethylhexyl Phthalate USDMF includes data on Diethylhexyl Phthalate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Diethylhexyl Phthalate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Diethylhexyl Phthalate suppliers with USDMF on PharmaCompass.
Diethylhexyl Phthalate 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 Diethylhexyl Phthalate 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 Diethylhexyl Phthalate GMP manufacturer or Diethylhexyl Phthalate GMP API supplier for your needs.
A Diethylhexyl Phthalate CoA (Certificate of Analysis) is a formal document that attests to Diethylhexyl Phthalate's compliance with Diethylhexyl Phthalate specifications and serves as a tool for batch-level quality control.
Diethylhexyl Phthalate CoA mostly includes findings from lab analyses of a specific batch. For each Diethylhexyl Phthalate 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.
Diethylhexyl Phthalate may be tested according to a variety of international standards, such as European Pharmacopoeia (Diethylhexyl Phthalate EP), Diethylhexyl Phthalate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Diethylhexyl Phthalate USP).