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API SUPPLIERS
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USDMF
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API/FDF Prices: Book a Demo to explore the features and consider upgrading later
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Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Regulatory Info : Allowed
Registration Country : Switzerland
Glucose; Sodium Chloride; Potassium Chloride; Sodium Citrate Dihydrate
Brand Name : Elotrans
Dosage Form : Powder For Oral Solution
Dosage Strength :
Packaging :
Approval Date : 17/03/1983
Application Number : 44644
Regulatory Info : Allowed
Registration Country : Switzerland
Regulatory Info : Deregistered
Registration Country : Sweden
Glucose (Anhydrous); Potassium Chloride; Sodium Citrate (Dihydrate); Sodium Chloride
Brand Name : Aqurex
Dosage Form : Powder For Oral Solution
Dosage Strength :
Packaging :
Approval Date : 28/06/2012
Application Number : 20110302000234
Regulatory Info : Deregistered
Registration Country : Sweden
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ABOUT THIS PAGE
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PharmaCompass offers a list of Glucose 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 Glucose manufacturer or Glucose supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glucose manufacturer or Glucose supplier.
PharmaCompass also assists you with knowing the Glucose API Price utilized in the formulation of products. Glucose API Price is not always fixed or binding as the Glucose Price is obtained through a variety of data sources. The Glucose Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DSSTox_CID_2910 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_2910, including repackagers and relabelers. The FDA regulates DSSTox_CID_2910 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_2910 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 DSSTox_CID_2910 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DSSTox_CID_2910 supplier is an individual or a company that provides DSSTox_CID_2910 active pharmaceutical ingredient (API) or DSSTox_CID_2910 finished formulations upon request. The DSSTox_CID_2910 suppliers may include DSSTox_CID_2910 API manufacturers, exporters, distributors and traders.
click here to find a list of DSSTox_CID_2910 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A DSSTox_CID_2910 DMF (Drug Master File) is a document detailing the whole manufacturing process of DSSTox_CID_2910 active pharmaceutical ingredient (API) in detail. Different forms of DSSTox_CID_2910 DMFs exist exist since differing nations have different regulations, such as DSSTox_CID_2910 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A DSSTox_CID_2910 DMF submitted to regulatory agencies in the US is known as a USDMF. DSSTox_CID_2910 USDMF includes data on DSSTox_CID_2910's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DSSTox_CID_2910 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of DSSTox_CID_2910 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 DSSTox_CID_2910 Drug Master File in Japan (DSSTox_CID_2910 JDMF) empowers DSSTox_CID_2910 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 DSSTox_CID_2910 JDMF during the approval evaluation for pharmaceutical products. At the time of DSSTox_CID_2910 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 DSSTox_CID_2910 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 DSSTox_CID_2910 Drug Master File in Korea (DSSTox_CID_2910 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of DSSTox_CID_2910. The MFDS reviews the DSSTox_CID_2910 KDMF as part of the drug registration process and uses the information provided in the DSSTox_CID_2910 KDMF to evaluate the safety and efficacy of the drug.
After submitting a DSSTox_CID_2910 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 DSSTox_CID_2910 API can apply through the Korea Drug Master File (KDMF).
click here to find a list of DSSTox_CID_2910 suppliers with KDMF on PharmaCompass.
A DSSTox_CID_2910 CEP of the European Pharmacopoeia monograph is often referred to as a DSSTox_CID_2910 Certificate of Suitability (COS). The purpose of a DSSTox_CID_2910 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DSSTox_CID_2910 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DSSTox_CID_2910 to their clients by showing that a DSSTox_CID_2910 CEP has been issued for it. The manufacturer submits a DSSTox_CID_2910 CEP (COS) as part of the market authorization procedure, and it takes on the role of a DSSTox_CID_2910 CEP holder for the record. Additionally, the data presented in the DSSTox_CID_2910 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DSSTox_CID_2910 DMF.
A DSSTox_CID_2910 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DSSTox_CID_2910 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of DSSTox_CID_2910 suppliers with CEP (COS) on PharmaCompass.
DSSTox_CID_2910 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 DSSTox_CID_2910 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 DSSTox_CID_2910 GMP manufacturer or DSSTox_CID_2910 GMP API supplier for your needs.
A DSSTox_CID_2910 CoA (Certificate of Analysis) is a formal document that attests to DSSTox_CID_2910's compliance with DSSTox_CID_2910 specifications and serves as a tool for batch-level quality control.
DSSTox_CID_2910 CoA mostly includes findings from lab analyses of a specific batch. For each DSSTox_CID_2910 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.
DSSTox_CID_2910 may be tested according to a variety of international standards, such as European Pharmacopoeia (DSSTox_CID_2910 EP), DSSTox_CID_2910 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DSSTox_CID_2910 USP).
