Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
FDF
0
Australia
DRUG PRODUCT COMPOSITIONS0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
API SUPPLIERS
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]
FDF Dossiers
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]FDA Orange Book
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Europe
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]Canada
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]DRUG PRODUCT COMPOSITIONS
DOSAGE - INJECTABLE;INJECTION - 469.01MG/ML
USFDA APPLICATION NUMBER - 19596
DOSAGE - INJECTABLE;INJECTION - 469.01MG/ML
USFDA APPLICATION NUMBER - 21037
Digital Content
NEWS #PharmaBuzz
Global Sales Information
Market Place
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Gadolinium Dtpa manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gadolinium Dtpa, including repackagers and relabelers. The FDA regulates Gadolinium Dtpa manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gadolinium Dtpa 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 Gadolinium Dtpa manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Gadolinium Dtpa supplier is an individual or a company that provides Gadolinium Dtpa active pharmaceutical ingredient (API) or Gadolinium Dtpa finished formulations upon request. The Gadolinium Dtpa suppliers may include Gadolinium Dtpa API manufacturers, exporters, distributors and traders.
click here to find a list of Gadolinium Dtpa suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Gadolinium Dtpa DMF (Drug Master File) is a document detailing the whole manufacturing process of Gadolinium Dtpa active pharmaceutical ingredient (API) in detail. Different forms of Gadolinium Dtpa DMFs exist exist since differing nations have different regulations, such as Gadolinium Dtpa USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Gadolinium Dtpa DMF submitted to regulatory agencies in the US is known as a USDMF. Gadolinium Dtpa USDMF includes data on Gadolinium Dtpa's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Gadolinium Dtpa USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Gadolinium Dtpa suppliers with USDMF on PharmaCompass.
Gadolinium Dtpa 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 Gadolinium Dtpa 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 Gadolinium Dtpa GMP manufacturer or Gadolinium Dtpa GMP API supplier for your needs.
A Gadolinium Dtpa CoA (Certificate of Analysis) is a formal document that attests to Gadolinium Dtpa's compliance with Gadolinium Dtpa specifications and serves as a tool for batch-level quality control.
Gadolinium Dtpa CoA mostly includes findings from lab analyses of a specific batch. For each Gadolinium Dtpa 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.
Gadolinium Dtpa may be tested according to a variety of international standards, such as European Pharmacopoeia (Gadolinium Dtpa EP), Gadolinium Dtpa JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Gadolinium Dtpa USP).
LOOKING FOR A SUPPLIER?
