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API SUPPLIERS
Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.
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USDMF
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Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.
About the Company : Pfanstiehl is a leader in high-purity, low endotoxin, low metals parenteral-grade excipient manufacturing for biologic formulations. The company’s expertise includes isolation, p...
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Global Sales Information
US Medicaid Prescriptions
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JP
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Sigma-Aldrich empowers scientific discovery with top-quality solutions to accelerate research, innovation, and better health worldwide.
CAS Number : 6363-53-7
Quantity Per Vial :
Sale Unit :
Price : $122.00
Details :
Monograph : PHR1497-1G
Storage : +2°C to +30°C
Code/Batch No :
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PharmaCompass offers a list of Maltose API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Maltose manufacturer or Maltose supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Maltose manufacturer or Maltose supplier.
A Sunmalt manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sunmalt, including repackagers and relabelers. The FDA regulates Sunmalt manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sunmalt 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 Sunmalt manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Sunmalt supplier is an individual or a company that provides Sunmalt active pharmaceutical ingredient (API) or Sunmalt finished formulations upon request. The Sunmalt suppliers may include Sunmalt API manufacturers, exporters, distributors and traders.
click here to find a list of Sunmalt suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Sunmalt DMF (Drug Master File) is a document detailing the whole manufacturing process of Sunmalt active pharmaceutical ingredient (API) in detail. Different forms of Sunmalt DMFs exist exist since differing nations have different regulations, such as Sunmalt USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sunmalt DMF submitted to regulatory agencies in the US is known as a USDMF. Sunmalt USDMF includes data on Sunmalt's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sunmalt USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sunmalt suppliers with USDMF on PharmaCompass.
Sunmalt 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 Sunmalt GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Sunmalt GMP manufacturer or Sunmalt GMP API supplier for your needs.
A Sunmalt CoA (Certificate of Analysis) is a formal document that attests to Sunmalt's compliance with Sunmalt specifications and serves as a tool for batch-level quality control.
Sunmalt CoA mostly includes findings from lab analyses of a specific batch. For each Sunmalt 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.
Sunmalt may be tested according to a variety of international standards, such as European Pharmacopoeia (Sunmalt EP), Sunmalt JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sunmalt USP).
