Synopsis
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USDMF
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JDMF
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EU WC
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KDMF
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NDC API
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VMF
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API
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FDF
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Listed Dossiers
DRUG PRODUCT COMPOSITIONS
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EDQM
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USP
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JP
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Drugs in Development
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDF Dossiers
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FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Related Excipient Companies
Evonik
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Nanjing Well Pharmaceutical
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Pfanstiehl
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Actylis
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Gangwal Chemicals
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Solubilizers
Parenteral
Thickeners and Stabilizers
Topical
Emulsifying Agents
Film Formers & Plasticizers
Taste Masking
Surfactant & Foaming Agents
Coating Systems & Additives
API Stability Enhancers
Co-Processed Excipients
Direct Compression
Rheology Modifiers
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ABOUT THIS PAGE
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PharmaCompass offers a list of Ustekinumab 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 Ustekinumab manufacturer or Ustekinumab supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ustekinumab manufacturer or Ustekinumab supplier.
PharmaCompass also assists you with knowing the Ustekinumab API Price utilized in the formulation of products. Ustekinumab API Price is not always fixed or binding as the Ustekinumab Price is obtained through a variety of data sources. The Ustekinumab Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ustekinumab manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ustekinumab, including repackagers and relabelers. The FDA regulates Ustekinumab manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ustekinumab 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 Ustekinumab manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ustekinumab supplier is an individual or a company that provides Ustekinumab active pharmaceutical ingredient (API) or Ustekinumab finished formulations upon request. The Ustekinumab suppliers may include Ustekinumab API manufacturers, exporters, distributors and traders.
click here to find a list of Ustekinumab suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
Ustekinumab 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 Ustekinumab 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 Ustekinumab GMP manufacturer or Ustekinumab GMP API supplier for your needs.
A Ustekinumab CoA (Certificate of Analysis) is a formal document that attests to Ustekinumab's compliance with Ustekinumab specifications and serves as a tool for batch-level quality control.
Ustekinumab CoA mostly includes findings from lab analyses of a specific batch. For each Ustekinumab 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.
Ustekinumab may be tested according to a variety of international standards, such as European Pharmacopoeia (Ustekinumab EP), Ustekinumab JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Ustekinumab USP).
