Microbiologics’ Post

Discover the latest insights into microbiological testing Nitto Avecia Pharma Services! Our comprehensive services ensure the highest quality and safety standards for your pharmaceutical products. Check out our in-depth article to learn more. #Pharma #Microbiology #QualityControl 

📚 Pre-order by 31 March to get a discounted rate on the new book on Industrial Pharmaceutical Microbiology Quality Control! This 500-page book is an in-depth, comprehensive survey of quality control pharma methods in the microbiology laboratory. The findings enable a better understanding of these quality control methods to ensure better developed, more compliant, and expedited procedures. This book is part of the Industrial Pharmaceutical Microbiology series and will be released on 01 April. https://bit.ly/48OVoD6 #PDA #microbiology

60 short tips implementing best practice in microbiological laboratory in Pharmaceutical industry

Bacterial endotoxin is the lipopolysaccharide (LPS) component of the cell wall of Gram-negative bacteria. It is pyrogenic. Pharmaceutical products that are injected into the human body are tested for pyrogenic substances. The most common, and arguably most important pyrogen, is bacterial endotoxin. Bacteria endotoxin presents a significant risk to many pharmaceutical products, especially parenteral products. This is because endotoxin is : ● ubiquitous in nature; ● has potent toxicity; ● is stable under extreme conditions; ● is likely to occur in the manufacturing process. The most common type of pyrogen found in the pharmaceutical industry is bacterial endotoxin, and for which, LAL is a specific test for. Moreover,there are alternatives to the LAL test such as, 1. Enzyme-linked Immunosorbent Assay (ELISA) methods and, 2. Monocyte Activation Test (MAT)

60 short tips implementing best practice in microbiological laboratory in Pharmaceutical industry

Short Tips for Implementing Best Practice in Microbiological Laboratory in Pharmaceutical Industry

📚 Pre-Order to Save: Industrial Pharmaceutical Microbiology Quality Control This 500-page book is an in-depth, comprehensive survey of quality control pharma methods in the microbiology laboratory. The findings enable a better understanding of these quality control methods to ensure better developed, more compliant, and expedited procedures. Pre-order by 31 March to get it at the discounted price of $269 – that’s 10% off. This book is part of the Industrial Pharmaceutical Microbiology series and will be released on 01 April. https://bit.ly/48OVoD6 #PDA #microbiology

📢 The recent announcement from US Pharmacopeia allowing the use of non-animal-derived reagents for endotoxin testing is a significant milestone for the pharmaceutical industry (https://lnkd.in/emRNwfXa). This change not only promotes ethical practices by reducing reliance on animal-derived products 🐰 but also enhances the consistency and reliability of testing outcomes 🔍. At QUALITY ASSISTANCE S.A., we are proud to be at the forefront of this advancement. Our state-of-the-art analytical services already include endotoxin testing using recombinant reagents 🧬, ensuring high precision and adherence to the latest industry standards. 📄 We invite you to explore our detailed application note on this topic, where we delve into the benefits and technical aspects of using alternative analytical solutions for endotoxin analysis. 🔗 Full application note available here: https://lnkd.in/eZZspM-P The brochure detailing the analytical services we offer for endotoxin testing is available here: https://lnkd.in/eGkAQW8V Together, let's drive innovation and quality in pharmaceutical testing 🚀. #PharmaceuticalTesting #QualityAssurance #EndotoxinTesting #Innovation #Sustainability

Pyrogen testing is important in the pharmaceutical industry because it detects the presence of pyrogens, which are substances that can cause fever. Pyrogens can contaminate pharmaceutical products during the manufacturing process and can cause serious health problems if they enter the body. Pyrogen testing helps to ensure the safety and quality of pharmaceutical products by detecting the presence of pyrogens and preventing their release into the market. The USP pyrogen test is a widely used method for detecting pyrogens, but it has some limitations, such as being time-consuming and requiring a large number of animals. The Bacterial Endotoxins Test (BET), also known as the Limulus Amebocyte Lysate (LAL) test, is a more sensitive and specific method that is widely used in the pharmaceutical industry. The BET is used to detect the presence of endotoxins, which are a type of pyrogen that is produced by gram-negative bacteria. The test is important because it helps to ensure the safety and quality of pharmaceutical products, and it is used to detect the presence of endotoxins in a wide range of products, including injectables, medical devices, and raw materials.

Interested in cutting-edge strategies for nitrosamine risk mitigation? Be sure to attend Zdravka Misic's poster presentation at the 14th Pharmaceutics, Biopharmaceutics and Pharmaceutical Technology (PBP) World Meeting in Austria (18-21 March)! Her technical poster elaborates on advantages of using ascorbic acid as a nitrite scavenger and nitrosamine mitigation agent. Discover how this simple solution could form part of your mitigation strategy and uncover how dsm-firmenich can support you in limiting nitrosamine contamination risk. We can’t wait to connect with you and explore the future of pharma together. See you there! #pharmaceutics #biopharmaceutics #pharmaceuticaltechnology #cannabinoids #nitrosamines #dsmfirmenichPharma