Synopsis
0
CEP/COS
0
JDMF
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
API
0
FDF
0
FDA Orange Book
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
EDQM
0
USP
0
JP
0
Others
0
US Patents
0
US Exclusivities
0
Health Canada Patents
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
US Medicaid
NA
Annual Reports
NA
Finished Drug Prices
NA
Digital Content 
DATA COMPILATION #PharmaFlow
NEWS #PharmaBuzz
ABOUT THIS PAGE
25
PharmaCompass offers a list of Lutetium Chloride Lu-177 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 Lutetium Chloride Lu-177 manufacturer or Lutetium Chloride Lu-177 supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lutetium Chloride Lu-177 manufacturer or Lutetium Chloride Lu-177 supplier.
PharmaCompass also assists you with knowing the Lutetium Chloride Lu-177 API Price utilized in the formulation of products. Lutetium Chloride Lu-177 API Price is not always fixed or binding as the Lutetium Chloride Lu-177 Price is obtained through a variety of data sources. The Lutetium Chloride Lu-177 Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lutetium Chloride Lu-177 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lutetium Chloride Lu-177, including repackagers and relabelers. The FDA regulates Lutetium Chloride Lu-177 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lutetium Chloride Lu-177 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Lutetium Chloride Lu-177 supplier is an individual or a company that provides Lutetium Chloride Lu-177 active pharmaceutical ingredient (API) or Lutetium Chloride Lu-177 finished formulations upon request. The Lutetium Chloride Lu-177 suppliers may include Lutetium Chloride Lu-177 API manufacturers, exporters, distributors and traders.
click here to find a list of Lutetium Chloride Lu-177 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lutetium Chloride Lu-177 DMF (Drug Master File) is a document detailing the whole manufacturing process of Lutetium Chloride Lu-177 active pharmaceutical ingredient (API) in detail. Different forms of Lutetium Chloride Lu-177 DMFs exist exist since differing nations have different regulations, such as Lutetium Chloride Lu-177 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lutetium Chloride Lu-177 DMF submitted to regulatory agencies in the US is known as a USDMF. Lutetium Chloride Lu-177 USDMF includes data on Lutetium Chloride Lu-177's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lutetium Chloride Lu-177 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lutetium Chloride Lu-177 suppliers with USDMF on PharmaCompass.
Lutetium Chloride Lu-177 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 Lutetium Chloride Lu-177 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 Lutetium Chloride Lu-177 GMP manufacturer or Lutetium Chloride Lu-177 GMP API supplier for your needs.
A Lutetium Chloride Lu-177 CoA (Certificate of Analysis) is a formal document that attests to Lutetium Chloride Lu-177's compliance with Lutetium Chloride Lu-177 specifications and serves as a tool for batch-level quality control.
Lutetium Chloride Lu-177 CoA mostly includes findings from lab analyses of a specific batch. For each Lutetium Chloride Lu-177 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.
Lutetium Chloride Lu-177 may be tested according to a variety of international standards, such as European Pharmacopoeia (Lutetium Chloride Lu-177 EP), Lutetium Chloride Lu-177 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lutetium Chloride Lu-177 USP).
