Synopsis
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CEP/COS
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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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FDF
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FDA Orange Book
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Europe
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Canada
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Australia
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South Africa
DRUG PRODUCT COMPOSITIONS
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EDQM
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USP
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JP
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Others
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US Patents
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US Exclusivities
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Health Canada Patents
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Stock Recap #PipelineProspector
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Weekly News Recap #Phispers
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News #PharmaBuzz
US Medicaid
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Annual Reports
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Finished Drug Prices
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API SUPPLIERS
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USDMF
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28729
Submission : 2014-12-11
Status :
Type : II
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Listed Suppliers
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
About the Company : Symbiotec, a leading API manufacturing company based in Indore, Central India, specializes in Cortico-Steroids and Steroid-Hormone APIs. Since 1995, their focus on R&D, sustainable...
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
About the Company : Established in 1994, Rochem is a distributor of pharmaceutical, food, nutritional and animal health ingredients to some of the largest companies in the world. It sources high-quali...
Pfizer CentreOne is a global CDMO and a leading supplier of Specialty APIs.
About the Company : Pfizer CentreOne® is an altogether different global contract development and manufacturing organization (CDMO), and a leading supplier of specialty APIs and intermediates.
...
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DATA COMPILATION #PharmaFlow
Market Place
ABOUT THIS PAGE
A CAS-853-23-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-853-23-6, including repackagers and relabelers. The FDA regulates CAS-853-23-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-853-23-6 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 CAS-853-23-6 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A CAS-853-23-6 supplier is an individual or a company that provides CAS-853-23-6 active pharmaceutical ingredient (API) or CAS-853-23-6 finished formulations upon request. The CAS-853-23-6 suppliers may include CAS-853-23-6 API manufacturers, exporters, distributors and traders.
click here to find a list of CAS-853-23-6 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A CAS-853-23-6 DMF (Drug Master File) is a document detailing the whole manufacturing process of CAS-853-23-6 active pharmaceutical ingredient (API) in detail. Different forms of CAS-853-23-6 DMFs exist exist since differing nations have different regulations, such as CAS-853-23-6 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A CAS-853-23-6 DMF submitted to regulatory agencies in the US is known as a USDMF. CAS-853-23-6 USDMF includes data on CAS-853-23-6's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The CAS-853-23-6 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of CAS-853-23-6 suppliers with USDMF on PharmaCompass.
CAS-853-23-6 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 CAS-853-23-6 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 CAS-853-23-6 GMP manufacturer or CAS-853-23-6 GMP API supplier for your needs.
A CAS-853-23-6 CoA (Certificate of Analysis) is a formal document that attests to CAS-853-23-6's compliance with CAS-853-23-6 specifications and serves as a tool for batch-level quality control.
CAS-853-23-6 CoA mostly includes findings from lab analyses of a specific batch. For each CAS-853-23-6 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.
CAS-853-23-6 may be tested according to a variety of international standards, such as European Pharmacopoeia (CAS-853-23-6 EP), CAS-853-23-6 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (CAS-853-23-6 USP).
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