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