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JDMF
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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
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.
About the Company : Transform your biologic formulations with Pfanstiehl, the industry leader in High-Purity Low Endotoxin Low Metals Parenteral grade excipient manufacturing. Our expertise spans isol...
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]API Reference Price
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REF. STANDARDS & IMPURITIES
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ABOUT THIS PAGE
A Sucrose API manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sucrose API, including repackagers and relabelers. The FDA regulates Sucrose API manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sucrose API 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 Sucrose API manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sucrose API supplier is an individual or a company that provides Sucrose API active pharmaceutical ingredient (API) or Sucrose API finished formulations upon request. The Sucrose API suppliers may include Sucrose API API manufacturers, exporters, distributors and traders.
click here to find a list of Sucrose API suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sucrose API DMF (Drug Master File) is a document detailing the whole manufacturing process of Sucrose API active pharmaceutical ingredient (API) in detail. Different forms of Sucrose API DMFs exist exist since differing nations have different regulations, such as Sucrose API USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Sucrose API DMF submitted to regulatory agencies in the US is known as a USDMF. Sucrose API USDMF includes data on Sucrose API's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Sucrose API USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Sucrose API suppliers with USDMF on PharmaCompass.
Sucrose API 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 Sucrose API 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 Sucrose API GMP manufacturer or Sucrose API GMP API supplier for your needs.
A Sucrose API CoA (Certificate of Analysis) is a formal document that attests to Sucrose API's compliance with Sucrose API specifications and serves as a tool for batch-level quality control.
Sucrose API CoA mostly includes findings from lab analyses of a specific batch. For each Sucrose API 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.
Sucrose API may be tested according to a variety of international standards, such as European Pharmacopoeia (Sucrose API EP), Sucrose API JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Sucrose API USP).
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