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ABOUT THIS PAGE
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PharmaCompass offers a list of 3-5-Diiodothyropropionic Acid 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 3-5-Diiodothyropropionic Acid manufacturer or 3-5-Diiodothyropropionic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred 3-5-Diiodothyropropionic Acid manufacturer or 3-5-Diiodothyropropionic Acid supplier.
PharmaCompass also assists you with knowing the 3-5-Diiodothyropropionic Acid API Price utilized in the formulation of products. 3-5-Diiodothyropropionic Acid API Price is not always fixed or binding as the 3-5-Diiodothyropropionic Acid Price is obtained through a variety of data sources. The 3-5-Diiodothyropropionic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DIPTA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DIPTA, including repackagers and relabelers. The FDA regulates DIPTA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DIPTA 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 DIPTA supplier is an individual or a company that provides DIPTA active pharmaceutical ingredient (API) or DIPTA finished formulations upon request. The DIPTA suppliers may include DIPTA API manufacturers, exporters, distributors and traders.
click here to find a list of DIPTA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DIPTA DMF (Drug Master File) is a document detailing the whole manufacturing process of DIPTA active pharmaceutical ingredient (API) in detail. Different forms of DIPTA DMFs exist exist since differing nations have different regulations, such as DIPTA USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DIPTA DMF submitted to regulatory agencies in the US is known as a USDMF. DIPTA USDMF includes data on DIPTA's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DIPTA USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of DIPTA 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 DIPTA Drug Master File in Japan (DIPTA JDMF) empowers DIPTA 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 DIPTA JDMF during the approval evaluation for pharmaceutical products. At the time of DIPTA 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 DIPTA suppliers with JDMF on PharmaCompass.
DIPTA 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 DIPTA 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 DIPTA GMP manufacturer or DIPTA GMP API supplier for your needs.
A DIPTA CoA (Certificate of Analysis) is a formal document that attests to DIPTA's compliance with DIPTA specifications and serves as a tool for batch-level quality control.
DIPTA CoA mostly includes findings from lab analyses of a specific batch. For each DIPTA 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.
DIPTA may be tested according to a variety of international standards, such as European Pharmacopoeia (DIPTA EP), DIPTA JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DIPTA USP).
