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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 Dipro manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dipro, including repackagers and relabelers. The FDA regulates Dipro manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dipro 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 Dipro supplier is an individual or a company that provides Dipro active pharmaceutical ingredient (API) or Dipro finished formulations upon request. The Dipro suppliers may include Dipro API manufacturers, exporters, distributors and traders.
click here to find a list of Dipro suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dipro DMF (Drug Master File) is a document detailing the whole manufacturing process of Dipro active pharmaceutical ingredient (API) in detail. Different forms of Dipro DMFs exist exist since differing nations have different regulations, such as Dipro USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dipro DMF submitted to regulatory agencies in the US is known as a USDMF. Dipro USDMF includes data on Dipro's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dipro USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dipro 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 Dipro Drug Master File in Japan (Dipro JDMF) empowers Dipro 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 Dipro JDMF during the approval evaluation for pharmaceutical products. At the time of Dipro 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 Dipro suppliers with JDMF on PharmaCompass.
Dipro 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 Dipro 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 Dipro GMP manufacturer or Dipro GMP API supplier for your needs.
A Dipro CoA (Certificate of Analysis) is a formal document that attests to Dipro's compliance with Dipro specifications and serves as a tool for batch-level quality control.
Dipro CoA mostly includes findings from lab analyses of a specific batch. For each Dipro 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.
Dipro may be tested according to a variety of international standards, such as European Pharmacopoeia (Dipro EP), Dipro JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Dipro USP).
