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