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Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Ethical
Registration Country : Canada
Brand Name : RESONIUM CALCIUM
Dosage Form : POWDER FOR SOLUTION
Dosage Strength : 999MG/G
Packaging : 300G
Approval Date :
Application Number : 2017741
Regulatory Info : Ethical
Registration Country : Canada
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Octavius has been empowering lives since 1980 by providing quality products like DC granules, APIs and FDFs.
Regulatory Info :
Registration Country : India
Brand Name : Calcium Polystyrene Su...
Dosage Form : Oral Powder
Dosage Strength :
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
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ABOUT THIS PAGE
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PharmaCompass offers a list of Calcium Polystyrene Sulfonate 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 Calcium Polystyrene Sulfonate manufacturer or Calcium Polystyrene Sulfonate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Calcium Polystyrene Sulfonate manufacturer or Calcium Polystyrene Sulfonate supplier.
PharmaCompass also assists you with knowing the Calcium Polystyrene Sulfonate API Price utilized in the formulation of products. Calcium Polystyrene Sulfonate API Price is not always fixed or binding as the Calcium Polystyrene Sulfonate Price is obtained through a variety of data sources. The Calcium Polystyrene Sulfonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Polystyrene Sulfonic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Polystyrene Sulfonic Acid, including repackagers and relabelers. The FDA regulates Polystyrene Sulfonic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Polystyrene Sulfonic 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 Polystyrene Sulfonic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Polystyrene Sulfonic Acid supplier is an individual or a company that provides Polystyrene Sulfonic Acid active pharmaceutical ingredient (API) or Polystyrene Sulfonic Acid finished formulations upon request. The Polystyrene Sulfonic Acid suppliers may include Polystyrene Sulfonic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Polystyrene Sulfonic Acid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Polystyrene Sulfonic Acid DMF (Drug Master File) is a document detailing the whole manufacturing process of Polystyrene Sulfonic Acid active pharmaceutical ingredient (API) in detail. Different forms of Polystyrene Sulfonic Acid DMFs exist exist since differing nations have different regulations, such as Polystyrene Sulfonic Acid USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Polystyrene Sulfonic Acid DMF submitted to regulatory agencies in the US is known as a USDMF. Polystyrene Sulfonic Acid USDMF includes data on Polystyrene Sulfonic Acid's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Polystyrene Sulfonic Acid USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Polystyrene Sulfonic Acid 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 Polystyrene Sulfonic Acid Drug Master File in Japan (Polystyrene Sulfonic Acid JDMF) empowers Polystyrene Sulfonic Acid 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 Polystyrene Sulfonic Acid JDMF during the approval evaluation for pharmaceutical products. At the time of Polystyrene Sulfonic Acid 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 Polystyrene Sulfonic Acid suppliers with JDMF 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 Polystyrene Sulfonic Acid Drug Master File in Korea (Polystyrene Sulfonic Acid KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Polystyrene Sulfonic Acid. The MFDS reviews the Polystyrene Sulfonic Acid KDMF as part of the drug registration process and uses the information provided in the Polystyrene Sulfonic Acid KDMF to evaluate the safety and efficacy of the drug.
After submitting a Polystyrene Sulfonic 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 Polystyrene Sulfonic Acid API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Polystyrene Sulfonic Acid suppliers with KDMF on PharmaCompass.
A Polystyrene Sulfonic Acid written confirmation (Polystyrene Sulfonic Acid WC) is an official document issued by a regulatory agency to a Polystyrene Sulfonic Acid manufacturer, verifying that the manufacturing facility of a Polystyrene Sulfonic Acid active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Polystyrene Sulfonic Acid APIs or Polystyrene Sulfonic Acid finished pharmaceutical products to another nation, regulatory agencies frequently require a Polystyrene Sulfonic Acid WC (written confirmation) as part of the regulatory process.
click here to find a list of Polystyrene Sulfonic Acid suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Polystyrene Sulfonic Acid as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Polystyrene Sulfonic Acid API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Polystyrene Sulfonic Acid as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Polystyrene Sulfonic Acid and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Polystyrene Sulfonic Acid NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Polystyrene Sulfonic Acid suppliers with NDC on PharmaCompass.
Polystyrene Sulfonic 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 Polystyrene Sulfonic 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 Polystyrene Sulfonic Acid GMP manufacturer or Polystyrene Sulfonic Acid GMP API supplier for your needs.
A Polystyrene Sulfonic Acid CoA (Certificate of Analysis) is a formal document that attests to Polystyrene Sulfonic Acid's compliance with Polystyrene Sulfonic Acid specifications and serves as a tool for batch-level quality control.
Polystyrene Sulfonic Acid CoA mostly includes findings from lab analyses of a specific batch. For each Polystyrene Sulfonic 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.
Polystyrene Sulfonic Acid may be tested according to a variety of international standards, such as European Pharmacopoeia (Polystyrene Sulfonic Acid EP), Polystyrene Sulfonic Acid JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Polystyrene Sulfonic Acid USP).
