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