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Injectable Pharmaceutical Articles & Analysis

10 articles found

Rethinking WFI Endotoxin Testing: From Lab Errors to Reliable Results

Rethinking WFI Endotoxin Testing: From Lab Errors to Reliable Results

Introduction: The Challenge of Endotoxin in WFI Endotoxin contamination in Water for Injection (WFI) is a critical concern in pharmaceutical laboratories. Even minor errors in endotoxin water testing can compromise product safety and regulatory compliance. WFI is used directly or indirectly in injectable products, making its purity paramount. ...

ByCreative BioMart


Continuous Microbial Monitoring in Aseptic Manufacturing Cleanrooms Following EU GMP Annex1:2020, ISO 14698:2003 & EN17141:2020

Continuous Microbial Monitoring in Aseptic Manufacturing Cleanrooms Following EU GMP Annex1:2020, ISO 14698:2003 & EN17141:2020

Overview Contamination Free Manufacturing (CFM) of Sterile injectable pharmaceutical products has historically involved particle control and removal. ...

ByLighthouse Worldwide Solutions (LWS)


Long-lasting Controlled-release Microspheres Technology

Long-lasting Controlled-release Microspheres Technology

The field of pharmaceuticals has seen rapid advancements in drug delivery technologies in recent years, one of which is long-lasting controlled-release microspheres technology. ...

ByCD Formulation


Food and beverage pharmaceutical pure water treatment

Food and beverage pharmaceutical pure water treatment

It is suitable for water supply treatment in electronics, medicine, chemical industry, thermal power generation, food, beer, beverage, printing and dyeing and coating industries, such as food pure water treatment, beverage pure water treatment, pharmaceutical pure water treatment and other pure water and high-purity water preparation. ...

ByGuangdong Stark Water Treatment Technology Co., Ltd.


What Is Drug Stability Analysis? - Basics You Need to Know in Drug Discovery

What Is Drug Stability Analysis? - Basics You Need to Know in Drug Discovery

The stability of pharmaceutical preparations directly affects the effectiveness and safety of drugs. Therefore, it is of great significance to study the stability of pharmaceutical preparations to ensure product quality, safety, and effectiveness. ...

ByCD Formulation


Regulatory Guidelines for API-Excipient Compatibility Studies

Regulatory Guidelines for API-Excipient Compatibility Studies

Classified by function and purpose, pharmaceutical excipients can be used in different drug forms, including: Injection, where pharmaceutical excipients are antioxidants, cosolvents, and isotonic regulators, etc. Oral solid preparations, where pharmaceutical excipients are lubricants, fillers, and adhesives and diluents, etc. ...

ByCD Formulation


Meco`s Masterfit System Selected for Nexus Pharmaceutical Facility

Meco`s Masterfit System Selected for Nexus Pharmaceutical Facility

” —George Gsell, MECO President Nexus Pharmaceuticals, maker of difficult-to-manufacture, high quality, FDA-approved specialty and generic drugs, is opening a $250 million, U.S. based pharmaceutical manufacturing facility in Pleasant Prairie, WI. The company, which specializes in making critical-need injectable medications more ...

ByMECO Incorporated - A Grundfos Company


Applications of porous titanium

Applications of porous titanium

With its unique properties, porous titanium can be widely used in the pharmaceutical industry, water treatment industry, food industry, bioengineering, chemical industry, petrochemical, metallurgical industry and gas purification. ...

ByEdgetech Industries LLC


Abstract 15053: New Insights into the Development of the Protease Proprotein Convertase Subtilisin-Like Kexin Type 9 Antagonists

Abstract 15053: New Insights into the Development of the Protease Proprotein Convertase Subtilisin-Like Kexin Type 9 Antagonists

Secreted PCSK9 binds to the LDL-receptor (LDLR) and chaperones it to the degradation pathway. Several pharmaceutical companies have developed injectable mAb PCSK9 antagonists. ...

ByShifa Biomedical Corporation


Simplifying the Process: Automated Pharmacopoeia Testing of Purified Water and Water for Injection

Simplifying the Process: Automated Pharmacopoeia Testing of Purified Water and Water for Injection

Abstract The requirements for Total Organic Carbon (TOC) analysis of Water for Injection (WFI) and pharmaceutical purified water (PW) are provided for in monographs of the United States Pharmacopoeia (USP) and European Pharmacopoeia (EP). ...

ByTeledyne Tekmar

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