Synopsis
0
USDMF
0
CEP/COS
0
EU WC
0
KDMF
0
NDC API
0
VMF
0
Listed Suppliers
0
EDQM
0
USP
0
JP
0
Others
0
FDF Dossiers
0
FDA Orange Book
0
Europe
0
Canada
0
Australia
0
South Africa
0
Listed Dossiers
DRUG PRODUCT COMPOSITIONS
0
US Patents
0
US Exclusivities
0
Health Canada Patents
US Medicaid
NA
Annual Reports
NA
Regulatory FDF Prices
NA
0
API
0
FDF
0
Data Compilation #PharmaFlow
0
Stock Recap #PipelineProspector
0
Weekly News Recap #Phispers
0
News #PharmaBuzz
ABOUT THIS PAGE
79
PharmaCompass offers a list of Mepitiostane 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 Mepitiostane manufacturer or Mepitiostane supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mepitiostane manufacturer or Mepitiostane supplier.
PharmaCompass also assists you with knowing the Mepitiostane API Price utilized in the formulation of products. Mepitiostane API Price is not always fixed or binding as the Mepitiostane Price is obtained through a variety of data sources. The Mepitiostane Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL, including repackagers and relabelers. The FDA regulates CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL 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 CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL supplier is an individual or a company that provides CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL active pharmaceutical ingredient (API) or CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL finished formulations upon request. The CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL suppliers may include CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL API manufacturers, exporters, distributors and traders.
click here to find a list of CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL Drug Master File in Japan (CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL JDMF) empowers CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL JDMF during the approval evaluation for pharmaceutical products. At the time of CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL suppliers with JDMF on PharmaCompass.
CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL 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 CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL 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 CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL GMP manufacturer or CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL GMP API supplier for your needs.
A CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL CoA (Certificate of Analysis) is a formal document that attests to CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL's compliance with CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL specifications and serves as a tool for batch-level quality control.
CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL CoA mostly includes findings from lab analyses of a specific batch. For each CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL 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.
CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL may be tested according to a variety of international standards, such as European Pharmacopoeia (CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL EP), CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL JP (Japanese Pharmacopeia) and the US Pharmacopoeia (CYCLOPENTANONE 2.ALPHA.,3.ALPHA.-EPITHIO-5.ALPHA.-ANDROSTAN-17.BETA.-YL METHYL ACETAL USP).
