API Suppliers
US DMFs Filed
CEP/COS Certifications
0
JDMFs Filed
0
Other Certificates
0
Other Suppliers
USA (Orange Book)
0
Europe
0
Canada
0
Australia
0
South Africa
0
Uploaded Dossiers
U.S. Medicaid
0
Annual Reports
0
0
USFDA Orange Book Patents
0
USFDA Exclusivities
0
Blog #PharmaFlow
0
News
EDQM
0
USP
0
JP
0
Other Listed Suppliers
0
0
32
PharmaCompass offers a list of Biapenem 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 Biapenem manufacturer or Biapenem supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Biapenem manufacturer or Biapenem supplier.
PharmaCompass also assists you with knowing the Biapenem API Price utilized in the formulation of products. Biapenem API Price is not always fixed or binding as the Biapenem Price is obtained through a variety of data sources. The Biapenem Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Biapenem manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Biapenem, including repackagers and relabelers. The FDA regulates Biapenem manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Biapenem 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 Biapenem manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Biapenem supplier is an individual or a company that provides Biapenem active pharmaceutical ingredient (API) or Biapenem finished formulations upon request. The Biapenem suppliers may include Biapenem API manufacturers, exporters, distributors and traders.
click here to find a list of Biapenem suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Biapenem DMF (Drug Master File) is a document detailing the whole manufacturing process of Biapenem active pharmaceutical ingredient (API) in detail. Different forms of Biapenem DMFs exist exist since differing nations have different regulations, such as Biapenem USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Biapenem DMF submitted to regulatory agencies in the US is known as a USDMF. Biapenem USDMF includes data on Biapenem's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Biapenem USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Biapenem suppliers with USDMF on PharmaCompass.
Biapenem 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 Biapenem 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 Biapenem GMP manufacturer or Biapenem GMP API supplier for your needs.
A Biapenem CoA (Certificate of Analysis) is a formal document that attests to Biapenem's compliance with Biapenem specifications and serves as a tool for batch-level quality control.
Biapenem CoA mostly includes findings from lab analyses of a specific batch. For each Biapenem 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.
Biapenem may be tested according to a variety of international standards, such as European Pharmacopoeia (Biapenem EP), Biapenem JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Biapenem USP).